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PPAP: the complete guide

The production part approval process step by step: when you need it, how it runs, what each of the 18 elements contains, what the customer accepts, and how to get from the significant production run to a signed PSW.

Ľubomír Blažek
Process quality team leader, automotive · updated 2026-11-01

PPAP is the approval a supplier needs before it may ship series parts to an automotive customer. It answers two questions: does the supplier understand every requirement of the drawing and the specifications, and can the production process make conforming parts consistently at the quoted rate? The rules come from the AIAG PPAP manual (4th edition) plus the customer’s own requirements, which always take precedence.

When a PPAP is required

SituationExampleWhat to do
New part or productFirst production of a part numberSubmission
Engineering changeDrawing, specification or material changeSubmission
ToolingNew, additional, replaced or refurbished toolingSubmission
Tooling transferTools moved to another plant or lineSubmission
Production locationParts made at an additional or new siteSubmission
Sub-supplier or material sourceNew supplier of a component, material or service (e.g. heat treatment)Submission
Process changeChange in method, process parameters or sequenceSubmission
Tooling inactiveNo production for 12 months or moreSubmission
Correction of a discrepancyEarlier submission had an errorSubmission
Other changesChanges that do not affect fit, form or functionNotify the customer; they decide

When in doubt, notify the customer before the change and let them decide. Shipping changed parts without approval is one of the most serious supplier quality failures.

PPAP process flowchart

1Triggernew part, change,new site or supplier2Agreesubmission level,customer requirements3Plan18 elements: ownerand due date4APQP outputsflow chart, PFMEA,control plan5GaugesMSA for every gaugein the control plan6Production run1 to 8 h, at least300 parts, series tools7Resultsdimensions, material,performance, Ppk8Packageall elementsand the PSW9Submitwhat the level asks,retain the restCustomerdecisionapproved10Productionfollow the control plan,SPC, auditsinterim / rejected!Correctactions, deadline,then resubmitany later change: notify the customer, new PPAP if required (back to 1)
PPAP process: from the trigger to customer approval. Interim approval and rejection lead back to corrective actions; any later change starts the loop again.
  1. Trigger and agreement. Confirm with the customer that a PPAP is needed, the submission level, the number of sample parts and every customer-specific requirement.
  2. Plan. Give each of the 18 elements an owner and a due date, working back from the PPAP date in the APQP plan.
  3. APQP outputs. Process flow, PFMEA and control plan must be complete and consistent before the production run.
  4. Gauges. Measurement system analysis for every gauge in the control plan, so the results can be trusted.
  5. Significant production run. Production site, tools, process, materials and operators, at rate, typically 1 to 8 hours and at least 300 consecutive parts.
  6. Results and package. Dimensional, material and performance results, capability studies, then the package and the signed PSW.
  7. Customer decision. Approved, interim approval or rejected. Only full or interim approval allows series shipments.

Submission levels

LevelWhat goes to the customer
Level 1PSW only (and the appearance approval report where required)
Level 2PSW with product samples and limited supporting data
Level 3PSW with product samples and complete supporting data: the default
Level 4PSW and other requirements as defined by the customer
Level 5PSW with product samples and complete supporting data reviewed at the supplier’s manufacturing site

The level only decides what is sent. Every applicable element must exist at every level; retained elements are kept at your site and shown on request.

The 18 PPAP elements by level

S submit to the customer and retain · R retain and make available · * as the customer specifies

#ElementL1L2L3L4L5
1Design recordsRSS*R
2Authorized engineering change documentsRSS*R
3Customer engineering approvalRRS*R
4Design FMEARRS*R
5Process flow diagramRRS*R
6Process FMEARRS*R
7Control planRRS*R
8Measurement system analysis studiesRRS*R
9Dimensional resultsRSS*R
10Material / performance test resultsRSS*R
11Initial process studiesRRS*R
12Qualified laboratory documentationRSS*R
13Appearance approval report (AAR)SSS*R
14Sample production partsRSS*R
15Master sampleRRR*R
16Checking aidsRRR*R
17Customer-specific requirements recordsRRS*R
18Part Submission Warrant (PSW)SSSSR

What each element contains

  1. Design records: All released design records (drawings, CAD / math data, specifications) for the part and its components, marked with every characteristic numbered (ballooned).
  2. Authorized engineering change documents: Authorized engineering change documents for any change not yet included in the design record.
  3. Customer engineering approval: Evidence of customer engineering approval where the design record requires it (e.g. engineering trial runs, deviations).
  4. Design FMEA: Design FMEA when the supplier is design-responsible, using the AIAG-VDA method.
  5. Process flow diagram: Process flow diagram covering every step from receiving to shipping, including rework and nonconforming material.
  6. Process FMEA: Process FMEA for every operation, consistent with the flow diagram and the control plan.
  7. Control plan: Production control plan with all characteristics, controls, sample sizes, frequencies and reaction plans.
  8. Measurement system analysis studies: Measurement system analysis for every gauge and test equipment listed in the control plan (variable and attribute).
  9. Dimensional results: Dimensional results for every characteristic on the drawing, on the number of parts required by the customer (often 5 parts, each cavity and each process stream).
  10. Material / performance test results: Material, chemical, metallurgical and performance test results required by the design record and the control plan.
  11. Initial process studies: Initial process studies (Ppk) for special characteristics, from the significant production run.
  12. Qualified laboratory documentation: Scope and accreditation (e.g. ISO/IEC 17025) of the laboratories used for the tests.
  13. Appearance approval report (AAR): Appearance approval report for parts with appearance requirements (colour, grain, gloss).
  14. Sample production parts: Sample production parts as requested by the customer, from the significant production run.
  15. Master sample: Master sample kept by the supplier, signed off with the customer, for the life of the part.
  16. Checking aids: Part-specific checking aids (fixtures, templates, gauges) with their certification and MSA.
  17. Customer-specific requirements records: Records of compliance with all applicable customer-specific requirements.
  18. Part Submission Warrant (PSW): Part Submission Warrant summarising the submission, signed by an authorised person.

Acceptance criteria

CheckScopeTypical acceptance
Dimensional resultsEvery characteristic on the drawing, numbered (ballooned), on the parts the customer requestsAll within tolerance
Material and performance testsChemical, mechanical, durability and functional tests from the design record or DVP&RAll requirements met, by a qualified lab
Initial process studiesSpecial characteristics, from the significant production run (≥ 25 subgroups / 100 values)Ppk > 1.67 accepted; 1.33 to 1.67 after customer agreement; < 1.33 not accepted
Measurement system analysisEvery gauge and test listed in the control planTypically %GRR ≤ 10 %, 10 to 30 % with customer agreement; Cg, Cgk ≥ 1.33; kappa ≥ 0.75
AppearanceColour, gloss, grain, texture where the drawing requires itApproved appearance approval report
Run at rateOften required by the customer as part of the significant production runDemonstrated capacity ≥ quoted rate

Customer requirements override these values. Check capability with the Cpk calculator and gauges with the Gage R&R and type 1 study. More on Ppk: PPAP capability requirements.

Part Submission Warrant (PSW)

SectionContent
Part informationPart name and number, drawing revision and date, engineering change level, weight, safety / regulatory items, IMDS
Organization and customerSupplier name and site, customer, buyer / purchase order
Reason for submissionInitial submission, engineering change, tooling, correction, sub-supplier change, process change, additional location, other
Submission level1 to 5, as requested by the customer
Submission resultsDimensional, material / functional, appearance and statistical results: meet all requirements yes / no
DeclarationSigned by an authorized person: the samples are representative and made by a process that meets all PPAP requirements
Customer dispositionApproved, interim approval or rejected, with date and signature

One PSW per part number unless the customer agrees otherwise. If any result does not meet the requirement, say so on the PSW and explain it; never tick “yes” to make the package look complete.

Customer approval

DecisionMeaningNext step
ApprovedAll requirements metStart series shipments
Interim approvalShipments allowed for a limited time or quantityClose the actions and resubmit before it expires
RejectedRequirements not metCorrect, update the affected elements, resubmit; no series shipments

After approval

  • Produce exactly as approved: follow the control plan and keep the PFMEA and work instructions current.
  • Monitor special characteristics with SPC and keep Cpk at the agreed level.
  • Check daily that the standard is followed, for example with layered process audits.
  • Many customers require an annual layout inspection and functional verification of every part number.
  • Any change to product, process, tooling, material, sub-supplier or location: notify the customer first and resubmit when required.

Why PPAPs get rejected

  • Drawing revision on the PSW differs from the revision the parts were made to.
  • Characteristics on the ballooned drawing missing in the dimensional results, or results only “OK” without measured values.
  • Ppk from too few parts or from a run that was not with production tools, operators and rate.
  • Control plan, PFMEA and process flow do not match each other or the shop floor.
  • MSA missing for gauges named in the control plan, especially attribute (go / no-go and visual) checks.
  • Customer-specific requirements not addressed (labels, packaging, run at rate, annual layout).
  • A result that does not meet the requirement, with no explanation and no request for interim approval.

Create the PPAP online

All 18 elements, import of the FMEA, control plan, MSA and Ppk, what is missing for your level, and the complete PPAP with the PSW as one PDF. Free, no sign-up, data stays in your browser.

Open the PPAP tool →

FAQ

What is PPAP?

The production part approval process (AIAG) is how an automotive supplier proves, before series delivery, that it understands all customer requirements and that its production process makes conforming parts at the quoted rate. The result is a package of up to 18 elements and a signed Part Submission Warrant (PSW).

Which PPAP level should I use?

The one your customer asks for. Level 3 is the default in the AIAG PPAP manual when nothing else is specified.

What is a significant production run?

The run that produces the PPAP parts: typically 1 to 8 hours of production with at least 300 consecutive parts, on the production site, with production tooling, gauges, process, materials and operators, unless the customer specifies otherwise.

What is an interim approval?

A limited approval for a defined time or quantity while a requirement is not yet met, for example Ppk below 1.67. The supplier must have an action plan and resubmit before the interim approval expires.

Is PPAP required by IATF 16949?

IATF 16949 (8.3.4.4) requires a product and manufacturing process approval process that conforms to the customer requirements. For most North American customers that is PPAP; German OEMs usually require VDA PPF instead.

Can I create the PPAP online for free?

Yes. The QM Bench PPAP tool covers all 18 elements, imports the FMEA, control plan, MSA and Ppk from the other tools, shows what is still missing for your level and generates the complete package with the PSW as one PDF.

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