ISO 13485
Production Inspection Record
Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements.
Fully Customizable
Audit Ready
Instant Download
- Standard
- ISO 13485
- Document Type
- Records
- Format
- DOCX
- Language
- English
- Tags
- ISO 13485, Medical Devices, Records
This record documents the in-process and final inspection of one production lot.
What's Inside
- Purpose and Lot Identification
- Inspection Plan (ITP-1001)
- Incoming Material Status
- In-Process Inspection
- Dimensions (cm)
- Adhesive Strip
- Visual Inspection (100 %)
- Pouch Sealing
ISO 13485 Alignment
Supports ISO 13485:2016 requirements, including Clause 8.2.6. It fits with the rest of the QEHS Vault ISO 13485 document set.
Format
Supplied as a fully editable Microsoft Word (.docx) file. Add your organisation’s name, logo and details, then use it straight away. Instant download after purchase.
Key Benefits
- Professional, ready-to-use QEHS document designed to support effective implementation, documentation, and ongoing compliance with applicable management system requirements
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