Your Shopping Cart
13485 P-833 Product Recall and Advisory Notice
Format: MS Word
Language: English
Product Type: Digital
Provider: 13485 Store
Language: English
Product Type: Digital
Provider: 13485 Store
Price:
$39.00
Product Details
ISO 13485:2016 Procedure - Product Recall and Advisory Notice - describes the process used to determine and control the recall and withdrawal of medical devices for cause, the issuance of advisory notices, and generation of regulatory reports, if required. Addresses the Medical Device Report, outlines responsibilities of the Compliance Administrator and Committee, and covers Recall/Advisory Notices.
Customers Also Bought
- 13485:2003 to 2016 All-in-One Documentation and Training Transition Package (2003>>2016)
Price: $997 BUY NOW - 13185:2016 Flowcharts in MS Visio, SmartDraw, and PDF
Price: $109 BUY NOW - 13485:2016 Internal Auditor Tools: Checklist, Procedure and Forms
Price: $125 BUY NOW - Requirements of ISO 13485:2016 PPT Training Material
Price: $149 BUY NOW - ISO 13485:2016 Employee Training PPT
Price: $129 BUY NOW - 13485:2016 and FDA Compliant Gap Analysis Checklist
Price: $69 BUY NOW
You Recently Viewed