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Reviewed & edited by: Alvin Jin — IATF 16949 expert · Certified Product Engineering (PE) coach · DRBFM expert
Published 2024-01-04 · Last reviewed 2026-10-25
How to write and manage supplier corrective action reports using 8D methodology. Templates, worked examples, checklists and best practices for supplier quali...
A Supplier Corrective Action Report (SCAR) is a formal document sent by a customer to a supplier when a nonconformity is detected. Aligned with IATF 16949 Clause 10.2.4 and AIAG core tool standards, this guide provides a complete framework for supplier 8D response management. It requires the supplier to:
Most OEMs require suppliers to respond using the 8D methodology format.
SCAR = The REQUEST document sent TO the supplier 8D = The RESPONSE document sent BY the supplier
They are complementary: you issue a SCAR, the supplier responds with an 8D.
Issue a SCAR when:
Do NOT issue a SCAR for:
A complete SCAR response should include:
| Phase | Typical Timeline | Deliverable |
|---|---|---|
| Acknowledge | 24 hours | Receipt confirmation, initial containment status |
| D1-D3 | 24-48 hours | Team list, problem description, containment evidence |
| D4 | 5-10 working days | Root cause analysis with 5-Why |
| D5-D6 | 15-30 working days | Corrective action implementation |
| D7-D8 | 30-60 working days | Prevention, verification, closure |
A customer receives a shipment of machined brackets and finds a burr on the P3 edge during incoming inspection. The SQE issues a SCAR with this D2 statement: "0.5mm burr on Part X P3 edge, Lot#A938, 14 of 200 pieces affected, detected at customer incoming inspection on 12 March." The supplier's D3 containment quarantines 1,850 pieces in its warehouse and 600 pieces at the customer, sorts 100% with a deburr gauge, and declares a clean point at lot A941. D4 uses 5-Why and lands on a worn deburr tool that was not replaced at the defined interval, plus an escape point where the final visual check had no gauge and no sampling standard. D5-D6 replaces the tool on a fixed count-based interval, adds a deburr gauge to the final check, and records a 30-piece capability study of the edge dimension before and after. D7 updates the control plan and PFMEA and deploys the tool-interval change to two similar lines. D8 closes with the capability data, updated work instructions and a follow-up audit.
| Failure Mode | How to Detect It |
|---|---|
| Root cause stops at "operator error" | Ask what system allowed the error; a valid 5-Why ends at a process or design cause |
| Containment without a clean point | Request the sort quantity, date and the lot where containment ended |
| Corrective action with no verification | Look for capability or inspection data, not just a status field |
| Repeat SCAR on the same defect | Compare the new D4 with the previous one; if identical, D7 failed |
| Missing escape point | Check that D4 names both the occurrence cause and the escape cause |
Do not accept a SCAR response on the strength of its wording. Verify by re-checking the evidence: confirm the containment quantity matches the shipped quantity, confirm the clean point is traceable to a lot number, and confirm the D6 verification data comes from a capability study or a defined inspection sample rather than a single good part. For D8, request a follow-up audit or a sample of recent production data to show the fix holds over time. If the supplier cannot produce this, the SCAR stays open.
A SCAR is not a standalone document; it sits inside the wider 8D flow. D2 feeds directly into D4, because a vague problem statement produces a vague root cause. D3 containment protects the customer while D4 is being worked, and a weak D3 makes every later step unreliable. D5-D6 must trace back to the D4 root cause, and D7 must show the system change that prevents recurrence. D8 closes the loop by proving the fix works, which then feeds the next SCAR's D2 with better data.
Turn this method into a submittable 8D report
Generate a D0–D8 report skeleton with a 5-Why chain and containment actions.
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