§ 01 / WHAT

What PPAP accomplishes

PPAP is a structured way to prove you can manufacture parts consistently to spec. It covers:

  • Design understanding (drawings, specifications)
  • Process capability (process flow, FMEA, control plan)
  • Dimensional measurement (actual vs specified)
  • Material certification (MTRs, composition analysis)
  • Performance testing (durability, functional tests)
  • Appearance approval (for cosmetic parts)
  • Master sample retention (reference parts for comparison)

The customer reviews your submission. Approval signals "yes, we approve of your manufacturing setup for mass production of this part." Approval is specific to the drawing revision — any subsequent change requires new PPAP.

§ 02 / THE

The 5 PPAP levels

LevelRequirementTypical use case
Level 1Warrant only (no samples, minimal docs)Already-approved parts, minor revisions
Level 2Warrant + product samples (typically 3-5)Standard parts, low-risk applications
Level 3 (default)Warrant + samples + full documentation packageNew part approvals, most automotive submissions
Level 4Warrant + samples + docs + specified on-site testingCustomer-specific requirements
Level 5Everything from Level 4 + full test facility auditAerospace-adjacent applications, highest risk

Level 3 is the default for most automotive first-article approvals. Levels 1 and 2 are for lower-risk or reduced-complexity scenarios. Levels 4 and 5 add on-site verification beyond document review.

§ 03 / THE

The 18 PPAP elements (Level 3)

A complete Level 3 PPAP submission includes 18 specific elements:

  1. Design Record (engineering drawings, bill of material)
  2. Engineering Change Documents (if any design changes)
  3. Customer Engineering Approval
  4. Design Failure Mode and Effects Analysis (DFMEA)
  5. Process Flow Diagram
  6. Process Failure Mode and Effects Analysis (PFMEA)
  7. Control Plan
  8. Measurement System Analysis (MSA)
  9. Dimensional Results
  10. Records of Material / Performance Test Results
  11. Initial Process Studies (capability studies)
  12. Qualified Laboratory Documentation
  13. Appearance Approval Report (for cosmetic parts)
  14. Sample Production Parts
  15. Master Sample (retained by supplier)
  16. Checking Aids (gauges, fixtures used for inspection)
  17. Customer-Specific Requirements
  18. Part Submission Warrant (the cover document)

Each element is reviewed by the customer. Missing or inadequate documentation triggers rejection and rework — which can delay production by weeks.

§ 04 / EFFORT

Effort and cost

PPAP submissions take significant effort:

LevelTypical prep timeTypical cost (supplier-side)
Level 12-4 hours$200-400
Level 24-8 hours$400-800
Level 316-40 hours$1,500-4,000
Level 424-56 hours$2,500-6,000
Level 540+ hours, facility time$5,000-15,000

For custom parts in low volumes (under 500 units/year), PPAP cost may exceed the total part manufacturing cost. Specify PPAP level in the quote; many suppliers absorb Level 2 in standard pricing but Level 3+ requires explicit line-item cost.

§ 05 / WHEN

When to require which level

01

Level 1 or 2

Repeat orders of already-approved parts. Minor revisions (dimensional changes not affecting function). Parts from established suppliers with track record on similar work.

02

Level 3

New part introductions. New supplier qualifications. Safety-affected parts in consumer products. Standard automotive tier-2 supplies. Default for most commercial mass-produced components.

03

Level 4

Customer-specific testing requirements beyond standard PPAP. Specialty materials where composition verification needs outside testing. Applications near safety-critical thresholds.

04

Level 5

Safety-critical components (automotive airbag sensors, anti-lock brake components). Aerospace-adjacent applications. Specialized industries adopting PPAP from automotive. Requires supplier site visit and testing facility audit.

§ 06 / PPAP

PPAP vs AS9102 FAI vs ISO 13485

Different industries have similar-but-not-identical first-article documentation standards:

PPAP (AIAG): automotive default. Driven by quality metrics, process capability, and supplier self-reporting.

AS9102 First Article Inspection: aerospace equivalent. Similar structure but different emphases — more on dimensional verification, less on process capability statistics. Form 1 (accountability), Form 2 (product accountability), Form 3 (characteristic accountability).

ISO 13485 Design Controls: medical device. Structured around design verification and validation, risk management, usability engineering. More prescriptive on documented design history than PPAP.

All three share the underlying principle: prove manufacturing capability before production release. The specific documents differ by industry.

READY WHEN YOU ARE

PPAP submission to prepare?

Email [email protected]. We handle PPAP Levels 1-5 as part of our automotive IATF 16949-compliant process. Specify your required level and submission timeline.

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