Aerospace Sourcing
Procurement template: first article review

AS9102 First Article Report Review Checklist

Review an AS9102 first article inspection report in four passes: confirm the package is complete, check Form 1 identity and scope, trace every Form 2 material, process and test to a certificate, then match every balloon to a Form 3 line with a measured result and a suitable method. Each numbered item below gives a reason to accept or reject.

Updated

How to use this FAI review checklist

Use it line by line against the supplier's AS9102 first article inspection report (FAIR) before you sign Form 1 field 24. Every item is numbered so your team can write "FAI checklist item 17 not met" on a rejection notice instead of a paragraph of explanation.

The checklist follows the Revision C forms. SAE AS9102C was released in June 2023, and the form changes from Rev B are mostly on Form 1: field 14 became "Reason for Full / Partial FAI" and is required on every FAI, field 17 became "Part Type", field 18 became "FAIR Identifier", field 19 now asks whether the FAIR contains a documented nonconformance, and fields 20 and 22 are the reviewer and the approver, who should not be the same person. The signature blocks on Forms 2 and 3 were removed. Field numbers below follow the Rev C forms as described in published prime and supplier training; if your copy of the standard differs, the standard governs. Confirm the current revision on SAE before you adopt this.

For what an FAI is and when one is required, read our AS9102 first article inspection guide. This page assumes you know that and goes field by field. Two rules frame the whole review:

  • An FAI is not product acceptance. It verifies the production process. Each lot is still inspected and accepted.
  • Your PO decides scope. Prime clauses add to AS9102. Lockheed Martin Aeronautics quality clause Q2A Rev 17 (released 25 August 2025), for example, says it takes precedence over AS9102 where they conflict and must be read with it. Check the clauses you flowed down, at the revision on your PO.

Before you open the forms: package completeness

Reject an incomplete package before you review any numbers. A Form 3 you cannot check against a ballooned drawing is not reviewable.

#Field / clauseWhat to enter or requireWhy it matters / reference
1Forms 1, 2 and 3 presentAll three forms, or a stated reason a form is not applicable (for example, no material or special process in scope on Form 2)AS9102 report structure; Q2A Rev 17 para 4.P.1 requires approved Forms 1, 2 and 3 in the package
2Ballooned drawing or modelEvery design characteristic, including notes and flag notes, carries a unique balloon number; for model-based definition, a 2D representation of the model requirementsQ2A Rev 17 para 4.L requires ballooning of all design characteristics; para 4.P.3 requires a 2D representation of digital product definition requirements
3Supporting inspection reportsCMM reports, NDT reports and other data that back the Form 3 resultsQ2A Rev 17 para 4.P.5
4Material and process certificatesThe certs referenced on Form 2, in the order listed, annotated to the item where one cert covers severalLets you trace each Form 2 line to evidence; mirrors published supplier FAI submission checklists
5Sub-tier and sub-assembly FAIRsAn FAIR for each in-scope detail part or sub-assembly listed on Form 1, or the FAIR identifier of an existing approved oneQ2A Rev 17 para 4.G lets the buyer require FAIRs at all levels of indenture, including sub-tier suppliers
6Planning recordThe traveler or routing showing where each design characteristic is verified in productionQ2A Rev 17 para 4.P.2; the FAI must show the planned inspection steps will keep verifying conformity (para 3.B)
7Test dataAcceptance test procedure results, photos for visual characteristics, approvals required by the POQ2A Rev 17 para 4.P.4, 4.P.7 and 4.P.8
8Page countTotal pages stated, matching what you receivedA missing page is the most common reason a "complete" FAIR is not complete
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Form 1: part number accountability

Form 1 tells you what was inspected, at what configuration, and why. Most rejected FAIRs fail here, because the part number, revision or FAIR identifier does not match across the three forms.

#Field / clauseWhat to enter or requireWhy it matters / reference
9Fields 1, 2, 5: part number, name, revisionExactly as on the drawing and PO, including dash numberIf the drawing and PO disagree, stop and resolve it before reviewing further
10Fields 6, 7: drawing number and revisionThe drawing and revision used for the inspection; the supplier internal drawing if one existsConfirms the inspection was done to the configuration you bought
11Field 3: serial numberThe serial number of the unit inspected, or N/A if the part is not serializedTies the FAIR to one physical part
12Field 4: FAIR identifierSame identifier on all three forms and on attached reportsInconsistent identifiers across forms are a common rejection cause
13Field 8: additional changesEvery deviation, waiver, engineering order or unincorporated change that applies, or N/AApproved changes not listed here mean Form 3 may be inspecting the wrong requirement
14Fields 9 to 12: traveler, organization, supplier code, POProduction work order or lot, supplier name, your vendor code, your PO numberProves the part came from a production run under your order
15Field 13: detail or assemblyChecked correctly; an assembly needs the Form 1 index completedDrives whether fields 15 to 18 must be filled
16Field 14: full or partial, baseline, reasonFull or partial checked; for a partial, the baseline part number and revision and the baseline FAIR; the reason stated for every FAIRequired on all FAIs in Rev C; a partial with no baseline cannot be reviewed
17Fields 15 to 18: index of partsEvery sub-assembly, detail part, software item, standard catalog item and COTS item on the bill of materials, with part type and FAIR identifierRev C expects all BOM items, including COTS, listed; software needs its revision
18Field 19: documented nonconformanceYes or No, consistent with Form 3 field 11A Yes needs a disposition reference; a No with a nonconformance on Form 3 is a contradiction
19Fields 20 to 23: reviewed by, approved by, datesTwo different people, each identified, with datesRev C says the approver should not be the reviewer
20Fields 24, 25: customer approvalLeft blank for you; sign only after items 1 to 45 are metQ2A Rev 17 para 3.F: buyer approval does not transfer the seller's liability for FAI compliance
21Field 26: commentsNonconformance numbers, attached documents, and anything the reviewer must knowWhere suppliers should explain partial scope or open items

Form 2: materials, special processes and functional tests

Form 2 lists every raw material, special process and functional test the drawing or PO requires, each tied to a certificate or report. A Form 2 line with a spec and no certificate number is a claim, not evidence.

#Field / clauseWhat to enter or requireWhy it matters / reference
22Material or process name and specificationEach material and process with its spec number at the revision the drawing calls, for example "Ti-6Al-4V bar, AMS 4928" or "Fluorescent penetrant, ASTM E1417"Lets you compare the spec on Form 2 to the spec on the drawing; a different spec or revision needs an approved change
23Code and supplierAny class, type or grade code the spec requires, and the name of the mill, distributor or processorForm 2 field 8 identifies who supplied the material or did the process
24Customer approval verificationYes, No or N/A against your approved processor list where one appliesMany primes publish approved special process source lists; a source not on yours is a finding even if the work is good
25Certificate of conformance numberThe cert or report number for each line, matching an attached documentForm 2 field 10; the link between the FAIR and the evidence
26Heat, lot and date consistencyThe heat or lot on the material cert matches the traveler, and process cert dates fall inside the build windowA process cert dated before the part existed is a red flag, not a typo
27Functional test procedure and reportTest procedure number and acceptance report number for each required functional testForm 2 fields 11 and 12; Q2A treats acceptance test equipment and software as designed tooling (para 3.D)
28Special processor FAI or detailed CoCFor outside special processes, either a processor FAIR or a detailed CoC listing the process characteristics and resultsRev C explicitly applies to special processors and allows either route
29Embedded spec characteristicsCharacteristics inside material and process specs accounted for, by compliance matrix or equivalent, where your clauses require itQ2A Rev 17 para 3.A extends design characteristics to those embedded in Lockheed Martin M&P specifications, attached to Form 3

For reading the mill certs behind items 22 and 26, see material certs and traceability. For NDT callouts, see nondestructive testing.

Form 3: characteristic accountability

Form 3 must have one line for every balloon, with an actual result and the method used. Count balloons and count Form 3 lines first. If the numbers differ, return the FAIR.

#Field / clauseWhat to enter or requireWhy it matters / reference
30Field 5: characteristic numberOne line per balloon, numbered to match the drawing, including notes, general tolerances and flag notesDrawing notes left off Form 3 is the most common gap
31Field 6: reference locationDrawing zone or sheet and zone, for example "Sheet 2, C4"Lets a reviewer find the balloon quickly
32Field 7: characteristic designatorKey, critical or other designation from the drawing, or N/ACritical items often carry extra rules; Q2A Rev 17 para 4.E bars FAI by similarity for critical and interchangeable-replaceable items
33Field 8: requirementNominal and tolerance with units, for example "1.500 +/- .005 in"; notes may be abbreviatedCheck units against the drawing; inch and millimeter mixups survive casual review
34Field 9: resultsMeasured values for variable characteristics; for notes, "accepted", "applied" or the evidence reference; never just "OK"An attribute word where a measurement was possible is not objective evidence
35Field 10: designed or qualified toolingThe measuring method or equipment: CMM, micrometer, pin gauge, visual, test fixtureMethod must resolve the tolerance; calipers on a tight position tolerance are a red flag
36Field 11: nonconformance numberNCR number for any result outside tolerance, or N/AMust agree with Form 1 field 19
37Field 12: additional dataGauge ID and calibration due date for variable data; report numbers for notes verified by documentationLets you check the gauge was in calibration on the inspection date
38Out-of-tolerance resultsEvery reading against its tolerance, including ones the supplier marked acceptableDo the arithmetic yourself on critical and key characteristics
39Part markingMarking content, location and method verified, human and machine readableQ2A Rev 17 para 3.E applies part marking verification to both formats
40SoftwareSoftware or firmware part number and revision recorded and verified where the part contains itPublished supplier FAI training requires the software revision to be verified

Measurement method choice is covered in our inspection and metrology reference.

Full, partial and delta FAI: what triggers each

A full FAI covers every characteristic of a new part from a new source. A partial or delta FAI covers only what a change affects, and must reference the baseline FAIR it updates. Check field 14 against what actually changed.

Published prime and supplier FAI material lists these triggers for a new full or partial FAI:

#Field / clauseWhat to enter or requireWhy it matters / reference
41Design changePartial FAI covering changed characteristics, citing the engineering order or revisionChanges affecting fit, form or function
42Process, tooling, NC program or inspection method changePartial FAI on the affected characteristicsIncludes a change in material source; one published supplier guide requires a partial FAI when material moves from buyer-furnished to supplier-bought
43Change of manufacturing location or sourcePartial or full FAI as your clauses requireA move to a new site or a new sub-tier is a change of source
44Production lapseNew FAI after 24 months from the last production operation to restart, or the period your PO setsYour clauses may set a shorter period
45Natural or man-made event, or corrective actionPartial or full FAI covering what the event or the corrective action changedA corrective action that changes the process changes what the FAI verified

Prime clauses add conditions. Under Q2A Rev 17, the seller notifies the buyer's SQE in writing at least five business days before starting FAI planning, before inspecting the first production run, and before implementing any change that triggers a partial or re-accomplished FAI (para 4.A). FAI by similarity needs prior written approval and is never allowed for interchangeable-replaceable or critical items (para 4.E). An FAI the seller performed for another customer is accepted if it meets AS9102 and Q2A and is within two years of the PO, or older with evidence of continuous production to the same configuration (para 4.B). Q2A also lets the buyer require a new FAI for lost records or a nonconformance showing a characteristic was never accounted for (para 4.H). Unless the PO says otherwise, Q2A excludes metallic and non-metallic raw material, items returned for repair or rework, and tooling (para 1.E).

COTS items and standard catalog hardware normally do not get their own FAIR, but they belong in the Form 1 index. If the supplier modifies a COTS item to your requirements, the modification needs an FAI.

Common reasons to reject an FAIR

Reject, or return for correction, when the report cannot prove that every requirement was verified on a production part. These are the failures most often named in published supplier FAI training and prime clauses.

  1. Balloon count does not match Form 3 line count, usually missing drawing notes.
  2. Part number, revision or FAIR identifier differs between forms.
  3. Results recorded as "OK", "conforms" or a check mark where a value could be measured.
  4. Form 2 lists a spec with no certificate number, or a cert that is not attached.
  5. Spec revision on Form 2 differs from the drawing with no approved change in field 8.
  6. A partial FAI with no baseline FAIR identified, or with a reason that does not match the characteristics inspected.
  7. The FAI was run on a prototype, a hand-built part or residual inventory instead of the first production run.
  8. Measurement method too coarse for the tolerance, or gauges past their calibration due date.
  9. Nonconformance on Form 3 with no NCR number, or Form 1 field 19 marked No.
  10. Sub-assembly or outside process FAIRs missing for items listed on Form 1.
  11. Reviewer and approver are the same person.
  12. Special process done by a source not on your approved list.

Nonconformances found during the FAI are dispositioned under your normal nonconformance process. Q2A Rev 17 para 4.I points to AS9102 and Appendix QX for that, and delivery of nonconforming product needs an approved variance. See corrective action and SCAR when a rejection points to a systemic cause.

Records to keep after you approve

Keep the approved FAIR, every attachment and your review record for the retention period in your contract, and require the supplier to do the same. The FAIR is the baseline every later partial FAI points back to, so losing it can force a full FAI.

  • Your file: the signed Form 1, the full package as received, your checklist with item numbers marked, any rejection notices and the supplier responses.
  • Supplier retention: state a period on the PO. Lockheed Martin Missiles and Fire Control quality PO notes, for example, include a note setting 7 years for inspection and test records and 3 years for calibration records unless the purchasing requirements say otherwise, and L3Harris (Aerojet Rocketdyne) AR2 requires the buyer's written approval before any records are destroyed.
  • Change trail: link each partial FAI to its baseline and to the engineering order or process change behind it. Our records and change control reference covers the wider system.

If your supplier holds Nadcap accreditation for first article inspection, note it. Q2A Rev 17 para 1.G makes sellers accredited to AC7150 and the Lockheed Martin supplement eligible for FAI acceptance delegation on Lockheed Martin designed product.

What to put on the PO or RFQ about FAI

Say exactly what you will review, so the supplier prices it and builds the package to this list the first time.

  1. "First article inspection required to SAE AS9102 at the revision in effect on the PO date, on the first production run."
  2. Full or partial, and for a partial, the baseline FAIR identifier.
  3. Submission before shipment, and how long you need to review.
  4. Package contents: Forms 1 to 3, ballooned drawing, inspection reports, material and process certs, sub-tier FAIRs, test data.
  5. Your customer's clause by number and revision, for example "Lockheed Martin Q2A Rev 17 applies" when it flows to you.
  6. Advance notice of planning, inspection start and changes, with your lead time.
  7. Approved special process sources.
  8. Record retention period.

The RFQ builder and the aerospace RFQ checklist put this next to drawings, material and export classification. Pair this checklist with our certificate of conformance and trace package template for the paperwork that ships with every lot after the FAI.

How to adapt this checklist

Copy the numbered items into your own receiving or supplier quality procedure, then add your customer's clauses on top. Delete items that do not apply to your commodity and add commodity items, for example layer-by-layer data for printed circuit boards or weld maps for welded assemblies.

Keep the numbering stable once suppliers start seeing it, so "item 30" means the same thing next year. Review the checklist against each new revision of AS9102 and of the prime clauses you flow down. This template is a starting point and must be reviewed by your own contracts and quality teams before use. We do not give legal advice, and the standard and your contract govern where they differ from this page.

Get parts delivered with an FAIR that passes this review

Send the drawing, your quality clauses and this checklist through the inspection quote request. A person replies within 1 business day. We flow your AS9102 and clause requirements down to the supplier, review the FAIR against them before anything ships, and send every order with a certificate of conformance plus the other certs your request requires. If the drawing is export controlled, read confidentiality and controlled programs first.

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Part, quantity and date are enough to start. Drawings and the mutual NDA follow by reply, and controlled programs never send technical data through this site.

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Questions

What should a buyer check first on an AS9102 FAI report?

Check completeness before content. Confirm Forms 1, 2 and 3 are present, the ballooned drawing is attached, and the number of balloons equals the number of Form 3 lines. Then confirm the part number, revision and FAIR identifier match on all three forms and on your PO. If any of those fail, return the report before reviewing measurements, because nothing after that point can be traced reliably.

What changed on the AS9102 forms in Revision C?

Most changes are on Form 1. Field 14 became Reason for Full or Partial FAI and is required on every FAI, field 17 became Part Type, field 18 became FAIR Identifier, field 19 asks whether the FAIR contains a documented nonconformance, and fields 20 and 22 are the reviewer and approver, who should be different people. The signature blocks on Forms 2 and 3 were removed. Revision C was released in June 2023.

Can a supplier write OK instead of a measured value on Form 3?

Not for a characteristic that can be measured. Form 3 field 9 should hold the actual result for variable characteristics, and field 10 the method or equipment used. Words such as accepted or applied are normal for drawing notes, and a reference to the evidence document is acceptable where a note is verified by documentation. A check mark against a toleranced dimension is not objective evidence and is a common reason to reject.

When is a partial FAI acceptable instead of a full FAI?

When an earlier full FAI exists for the same part and only some characteristics are affected by a change, such as a design revision, a new tool, a new NC program, a new inspection method or a new material source. The partial must name the baseline FAIR and inspect every characteristic the change could affect. Some clauses require a full FAI for a site move or a long production lapse, so check yours.

Do outside special processes need their own FAI?

Revision C explicitly applies to special processors. The requirement can be met either by the processor producing its own FAIR or by a detailed certificate of conformance that lists the process characteristics and results. Your Form 2 review should confirm one of those is attached for each outside process, that the processor is on your approved list where one applies, and that the cert dates fit the build.

Does the buyer signing Form 1 make the buyer responsible for the FAI?

Not under the prime clauses we have read. Lockheed Martin Aeronautics quality clause Q2A Rev 17 states that the buyer SQE signature in the customer approval block of Form 1 does not transfer or limit the seller's liability for FAI compliance. Your approval records that your review found the package acceptable. The supplier still owns the accuracy of the results and the conformity of every delivered part.

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