Supplier audit and corrective action report
Turns supplier-audit evidence into a structured audit report, classified findings, and corrective-action request with traceable requirements. Use for supplier qualification, periodic audits, quality-system reviews, and follow-up of supplier nonconformities.
Publicado 21 de ago de 2026 · Actualizado 26 de ago de 2026
Requisitos
Add the audit checklist, applicable standard, and severity scale. Define corrective-action due-date and closure rules. Specify supplier risk tiers and escalation roles. Provide the required report and register formats.
Documento de la habilidad
El SKILL.md completo que tu agente lee y sigue.
Supplier audit and corrective action report
Purpose
Provide a consistent, evidence-based view of supplier performance and the actions needed to close audit findings.
Scope
Supplier quality, process, documentation, and control audits against a defined checklist, standard, or customer requirement. Excluded: supplier communication, audit certification, and acceptance of corrective actions.
Data basis
- Audit checklist, notes and evidence, supplier record, prior findings, applicable standard, and corrective-action procedure.
- The fixed records, tables, or folders in the skill scope that hold the relevant history or schema.
Result
An audit report, findings sheet, corrective-action request, and follow-up register row.
Quality criteria
- Each finding cites the checklist item, evidence, and supplier location or process.
- Classifications use the defined severity vocabulary.
- Findings state requirement, condition, risk, and evidence gap.
- Each action has a measurable closure criterion and due date or missing value.
- Repeat findings are linked to prior reports.
Instructions
Write findings as condition versus requirement, not as opinion. Keep observations, nonconformities, and recommendations distinct. Apply the company severity rules and do not infer a certification status. Group duplicate evidence only when it supports the same condition. Link corrective actions to the finding identifier and state what evidence would demonstrate closure.
Adapt before use
Keep the source trail close to every conclusion and preserve the difference between a source fact, a calculated value, an assumption, and a recommendation. Use stable identifiers across the document and sheet so a reviewer can move from a summary statement to the underlying row and source. Prefer a complete, transparent partial result over a confident answer built on missing evidence.
- Add the audit checklist, applicable standard, and severity scale.
- Define corrective-action due-date and closure rules.
- Specify supplier risk tiers and escalation roles.
- Provide the required report and register formats.
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