Form · FRM-13
Nonconforming Work Report
Identification, evaluation of significance, decision on acceptability, customer notification and recall.
Purpose
Records nonconforming work from identification through significance evaluation, look-back, decision on acceptability, customer notification, resumption of work and the decision on corrective action, in accordance with clause 7.10.
What it covers
- 1. Description
- 2. Evaluation of significance (Technical Manager)
- 3. Look-back summary
- 4. Decision
- 5. Resumption and follow-up
- Authorisation
How to complete it
- 1.Raise the same day as detection; number NCW-YY-NNN. Anyone may raise; the Technical Manager evaluates.
- 2.Describe factually what did not conform (procedure, requirement, equipment, environment, person) and how it was detected.
- 3.Record containment: work stopped, item and equipment secured, certificates withheld, equipment labelled (FRM-21).
- 4.Evaluate significance: effect on results and uncertainty, customer use, isolated or systematic, period affected. Perform and attach the look-back list where a standard, procedure, spreadsheet or condition was wrong.
- 5.Record the decision (accept with justification / accept with increased uncertainty / rework / reject and recall), customer notifications, resumption authorisation and whether a CAR is raised.
Before you use it
- Replace every square-bracket token, starting with [LABORATORY NAME], [ADDRESS] and [EFFECTIVE DATE]. The full token list is in GD-01 Read Me First.
- Have the content technically reviewed against how your laboratory actually works, then approved by the responsible manager before it becomes a controlled document.
- Update the Word fields after editing so the table of contents and page numbers are correct: select all, then press F9.
- Record the document in your own document register and set its review date.
Related documents
- QM-01
Quality Manual
Top-level description of the management system against every clause of ISO/IEC 17025:2017.
- SOP-08
Control of Nonconforming Work
Identifying, evaluating, containing and resolving work that departs from procedures or customer requirements.
- CHK-01
ISO/IEC 17025:2017 Gap Analysis and Self-Assessment
Clause-by-clause self-assessment with evidence, gap and action columns.
- FRM-01
Master Document Register
Register of every controlled internal and external document with revision, status and distribution.
- FRM-02
Document Change Request
Request, impact assessment and approval of a change to a controlled document.
- FRM-03
Records Retention Schedule and Disposal Log
Retention periods by record type and a log of authorised disposals.
- FRM-04
Internal Audit Programme and Audit Plan
Annual audit programme covering every clause and activity, plus the plan for a single audit.
- FRM-05
Internal Audit Checklist
Clause-by-clause question set with evidence and finding columns for auditing against ISO/IEC 17025.