Information
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NONCONFORMANCE REPORT
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Client / Site
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Conducted on
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Location
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Section 1
SECTION 1: To be completed by initiator
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Initiator Name
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Title
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Select date
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Street Address
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City/State/Zip
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Phone
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FAX
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E-Mail
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Part/Process Name
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QTY Affected
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P.O. Number
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Part Number
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REV
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REV Date
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Nonconformance Type (Check All That Apply)
- Dimensional
- Process
- Procedure
- Documentation
- Purchase Order
- Material
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Description Of Nonconformance
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Delivery, Schedule Or Cost Impact
Section 2
Section 2: AM QUALITY NCR REVIEW
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Date
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QA Name
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NCR Rejected
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NCR Accepted
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QA Phone
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E-Mail
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Defect Code
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Forward To:
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Notes
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Department Code
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Nonconformance Category
- Critical
- Major
- Minor
- Concern
- Observation
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CRITICAL : Could lead to a life threatening product liability or extreme safety hazard situation. Review and response is required upon finding.
MAJOR: Proven to be systematic and in direct conflict with said standard requirement. Response and completion of action items is required within (2) working days.
CONCERN: Any set of circumstances, which although is not a Nonconformance, could lead to a Nonconformance within the quality system. Response is not required, but recommended as reviewed by the quality NCR Administrator or qualified as assigned delegate.
OBSERVATION: A positive or negative fact within the quality system. Response is not required, but recommended for continuous improvement as reviewed by the QA Administrator or qualified assigned delegate.
Section 3
Section 3: Corrective And Preventive Action (CAPA)
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Corrective Action
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Response Due By:
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Preventive Action
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Response By:
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Title
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Date
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Phone Number
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E-Mail
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Fax
Section 4
Section 4: Quality Review Of CAPA
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Disposition Notes:
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NCR Closed?
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Follow Up Audit Required?
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Audit Assigned To:
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Audit To Be Completed By:
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NCR Administrator:
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