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REGISTRY DE NO CONFORMING (NC) Docs 13.01 Rev.10 RECLAMATION A PROVENDER Ferraro 2005 NOKC792 N Informed: Provender: Cargo de Rechazo: 09/05/16 Tech NC: 509 BECOME, S.L. Description: F:53636 ; Bra
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01
Start by identifying the non-conformity or issue that needs to be documented in the registro de no conformidad.
02
Provide a detailed description of the non-conformity, including any relevant dates, locations, and individuals involved.
03
Analyze the root cause of the non-conformity and identify any contributing factors.
04
Propose corrective actions that can be taken to address the non-conformity and prevent it from recurring in the future.
05
Assign responsibilities to individuals or departments for implementing the corrective actions.
06
Set target dates for completing the corrective actions and monitor progress towards achieving them.
07
Document any additional observations or comments related to the non-conformity.
08
Review the completed registro de no conformidad for accuracy and completeness before submitting it for further action or review.

Who needs registro de no conformidad:

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Organizations that aim to maintain quality standards and ensure compliance with regulations may require a registro de no conformidad.
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Quality control and quality assurance teams within companies often use the registro de no conformidad to document and address non-conformities.
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External auditors or regulatory agencies may request to review the registro de no conformidad as part of their assessment process.
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