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[Checklists] Internal Audit IATF 16949

structured matrix for IATF 16949 internal audits, linking clauses, checklist questions, evidence required, and automotive-specific examples:

IATF 16949 Internal Audit Matrix

(Aligned with ISO 9001:2015 structure + IATF specific requirements)

Clause

Checklist Question

Evidence to Review

Automotive Example

Compliance (✔/✖)

4.1 Context

Has the organization identified internal/external issues affecting QMS?

SWOT analysis, PESTLE report.

OEM demand shifts to EVs impacting supply chain.

5.1 Leadership

Does top management review customer scorecards (PPM, OTIF)?

Management review records, customer dashboards.

Review of Ford’s monthly quality scorecard.

6.1 Risks

Are risks updated post-FMEA or recall?

Risk register, FMEA updates, 8D reports.

Updated PFMEA after battery connector recall.

✖ (Overdue)

7.1.5.1 MSA

Is GR&R ≤10% for critical characteristics?

MSA reports, gauge calibration records.

Caliper GR&R for hood thickness measurement.

8.3.5.1 APQP

Is APQP on schedule for new projects?

APQP timelines, phase-gate review minutes.

Delayed Phase 4 (Validation) for Tesla bumper.

8.5.1 SPC

Are control charts active for CCs (CpK ≥1.33)?

X-bar R charts, reaction plans.

Stamping force SPC out-of-control (no action).

8.7.1 NC

Are containment actions implemented within 24hrs?

Containment records, quarantine logs.

Held 200 defective headlamps (no root cause).

9.1.2 Customer Satisfaction

Is customer feedback analyzed quarterly?

Survey results, warranty claims analysis.

Toyota’s Q3-2023 defect trend report.

10.2.1 CAPA

Are CAPAs closed within 30 days?

CAPA log, verification records.

Open CAPA #45 (45 days overdue).

Automotive-Specific Focus Areas

  1. Process Audits (VDA 6.3)

    • P2-P7: Verify project planning, production controls (e.g., weld validations).

    • Evidence: Process FMEAs, control plans, operator certifications.

  2. CSRs (Customer-Specific Requirements)

    • Example: Ford’s Q1 Certification for suppliers.

    • Evidence: CSR compliance matrix, audit reports.

  3. Traceability

    • Clause 8.5.2: Full traceability for recalls (e.g., VIN-based tracking).

    • Evidence: Material batch logs, serial number records.

Evidence Types & Examples

Evidence Category

Examples

Documentation

Control Plans, FMEAs, PPAP submissions, SOPs.

Records

MSA reports, SPC charts, training logs, calibration certs.

Observations

Gemba walk findings, 5S compliance, visual management.

Digital

ERP/MES data (OEE, downtime), IoT sensor alerts.

Non-Conformance (NC) Grading

NC Level

Criteria

Example

Major

Impacts product safety/regulatory compliance.

No PFMEA for brake component (IATF 6.1.2.3).

Minor

Isolated lapse without systemic impact.

Missing calibration sticker on 1 gauge.

Opportunity for Improvement (OFI)

Best practice gaps.

No automated SPC alerts in press shop.

Audit Workflow

  1. Plan: Focus on high-risk areas (e.g., CCs, recalls).

  2. Check: Use checklists + VDA 6.3 for process audits.

  3. Report: Document NCs with evidence (photos, screenshots).

  4. Follow-up: Verify CAPA effectiveness in 30 days.

Templates & Tools

  • Audit Checklist Template: [Download Link]

  • VDA 6.3 Questionnaire: [Example]

  • Automated Tools: Intelex, Qualio, Siemens Teamcenter.

Need sector-specific checklists (e.g., Casting, Electronics) or CAPA

 
 
 

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