ISO 13485 Procedure 820-Post Production Feedback

Defines the process whereby post production experiences are evaluated and acted upon.

File Size: 271 KB
Format: Word
Language: English
Product Type: Procedures
Provider: 13485 Store

Price: $39.00
Product Details


  • Describes a documented feedback system to collect and review information about medical devices in post-production phases.
  • The information is evaluated for possible relevance to safety and device efficacy.


  • Customizable ISO 13485 Post Production Feedback Procedure
  • Quality Records Table
  • Customer Satisfaction Survey Form
  • Corrective Preventative Action Form

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