ISO 13485

Customer Complaint Form

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
Form
Format
DOCX
Language
English
Tags
Form, ISO 13485, Medical Devices

This form records each complaint from receipt to closure.

What's Inside

  • PART A — Receipt
  • PART B — Evaluation and Reportability
  • B1 Is it a complaint?
  • B2 Reportability
  • PART C — Investigation
  • PART D — Product Handling and Actions
  • PART E — Customer Communication
  • PART F — Review and Closure

ISO 13485 Alignment

Supports ISO 13485:2016 requirements, including Clause 8.2.2. 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