13485 P-820 Post Production Feedback
Procedure - Post Production Feedback - Includes forms: F-821-001 Customer Satisfaction Survey and Analysis, F-852-001 Corrective/Preventive Action Request, F-425-001 Quality Records table.
Format: MS Word
Language: English
Product Type: Digital
Provider: 13485 Store
Language: English
Product Type: Digital
Provider: 13485 Store
Price:
$35.00
Product Details
ISO 13485:2016 Procedure - Post Production Feedback - defines the process whereby post production experiences are evaluated and acted upon. 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.
Customers Also Bought
- 9001.2015-P-740-Communication
Price: $31 BUY NOW - 9001.2015-P-750-Control-of-documented-information
Price: $31 BUY NOW - 9001.2015-P-810-Operational-planning-and-control
Price: $31 BUY NOW - 9001.2015-P-820-Customer-related-processes
Price: $31 BUY NOW - 9001.2015-P-830-Design-and-development
Price: $31 BUY NOW - 9001.2015-P-840-Control-of-external-providers
Price: $31 BUY NOW
You Recently Viewed
