Traceability Audit Template (Free)
Audit – Traceability
The traceability audit is a live drill: pick a finished product and trace it back, pick a raw material and trace it forward. If it takes all day, your system needs work – and this audit will show you where.
A good auditor is curious, not hostile. Record what you actually observed, note the evidence, and agree corrective actions with the auditee before you leave the area.
1. Audit details
| Field | Details |
|---|---|
| Audit title | Audit – Traceability |
| Audit no. | [AUD-YYYY-###] |
| Date(s) | [YYYY-MM-DD] |
| Auditor(s) | [Name(s)] |
| Area / process audited | [Area] |
| Auditee(s) | [Name(s) / Title(s)] |
2. Audit criteria
Reword the clauses to match your standard if you need to – but keep the numbering stable so you can trend findings over time.
| Ref | Requirement | C / NC / N/A | Evidence seen | Corrective action ref |
|---|---|---|---|---|
| 1.1 | Traceability procedure defines scope, responsibilities, and time targets. | |||
| 1.2 | Lot coding on finished product is legible and links to production records. | |||
| 1.3 | Raw material lot codes are captured at goods-in and linked to production. | |||
| 2.1 | Backward trace (finished product to suppliers) completes within the target time. | |||
| 2.2 | Forward trace (raw material to customers) completes within the target time. | |||
| 2.3 | Mass balance reconciles within acceptable tolerance. | |||
| 3.1 | Rework is traceable and its allergen status is identified. | |||
| 3.2 | Customer and supplier contact lists are current for recall purposes. | |||
| 3.3 | Traceability is tested at the defined frequency with records kept. | |||
| 4.1 | Gaps found in testing are corrected with preventive action. |
3. Summary
- Total clauses checked:
- Compliant: Non-compliant: N/A:
- Overall result: [Pass / Conditional pass / Fail – define your scoring rule here]
- Key strengths:
- Priority corrective actions: [list CAR references]
Approval and control
| Role | Name | Signature | Date |
|---|---|---|---|
| Prepared by | [Name] | [Signature] | [Date] |
| Reviewed by (QA) | [Name] | [Signature] | [Date] |
| Approved by | [Name] | [Signature] | [Date] |
Keep completed forms for [Define retention period, e.g., 2 years beyond shelf life] at [defined location] – and make sure someone besides you knows where that is.