Nonconforming Material Procedure | ISO 13485 | FDA QSR Compliant

$149.00
$149.00
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The ISO 13485 Nonconforming Material Procedure establishes a process to control and disposition nonconforming material identified during receiving, in-process, or final product acceptance activity.
  • ISO 13485:2016 Compliant
  • FDA QSR Compliant
  • Includes Related Forms
  • MS Word Format
  • Digital Content - Instant Download
SKU: SOP 8-008

Nonconforming Material Procedure

The Nonconforming Material Procedure establishes the process used to control and disposition nonconforming materials. The nonconforming material procedure applies to all nonconforming material or products identified during receiving, in-process, or final product acceptance activity. 

Nonconforming Material Procedure - Overview

​The Nonconforming Material Procedure governs failure of a raw material, component, sub-assembly, or finished product to meet an applicable specification. The Nonconforming Material Procedure provides instruction on identification of nonconforming material, segregation of discrepant product, and the methods of disposition of rejected product by qualified staff. The Nonconforming Material Procedure also includes a NCMR Report Form.

Nonconforming Material Procedure - Compliance

The Nonconforming Material Procedure is FDA QSR and ISO 13485:2016 compliant
To learn more about our ISO 13485 Nonconforming Material Procedure contact us at [email protected]

RELATED LINKS

​Corrective and Preventive Action Procedure
Lot Inspection Procedure
Identification Procedure
​​Medical Device Quality Management System MANUFACTURING
​Medical Device Quality Management System MANUFACTURING PLUS
ISO 13485 Nonconforming Material Procedure
NCMR Procedure

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