Information

  • NONCONFORMANCE REPORT

  • Client / Site

  • Conducted on

  • Location
  • Add media

Section 1

SECTION 1: To be completed by initiator

  • Initiator Name

  • Title

  • Select date

  • Street Address

  • City/State/Zip

  • Phone

  • FAX

  • E-Mail

  • Part/Process Name

  • QTY Affected

  • P.O. Number

  • Part Number

  • REV

  • REV Date

  • Nonconformance Type (Check All That Apply)

  • Description Of Nonconformance

  • Delivery, Schedule Or Cost Impact

Section 2

Section 2: AM QUALITY NCR REVIEW

  • Date

  • QA Name

  • NCR Rejected

  • NCR Accepted

  • QA Phone

  • E-Mail

  • Defect Code

  • Forward To:

  • Notes

  • Department Code

  • Nonconformance Category

  • 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)

  • Corrective Action

  • Response Due By:

  • Preventive Action

  • Response By:

  • Title

  • Date

  • Phone Number

  • E-Mail

  • Fax

Section 4

Section 4: Quality Review Of CAPA

  • Disposition Notes:

  • NCR Closed?

  • Follow Up Audit Required?

  • Audit Assigned To:

  • Audit To Be Completed By:

  • NCR Administrator:

  • Add signature

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