CalibrationObservationOpportunityForImprovement(OFI)SupplierNonconformanceCorrectiveandPreventiveAction(CAPA)ComplaintQuarantineReworkCertificate ofConformance(CoC)PreventiveMaintenanceRiskAssessmentGoodDocumentationPractice (GDP)InternalAuditQualityPolicyNonconformingMaterialDesignTransferCritical toQuality(CTQ)TrainingFileChangeOrder(CO)SeverityExternalAuditDeviceMasterRecord(DMR)ContinuousImprovementRootCauseFood andDrugAdministration(FDA)InternationalOrganizationforStandardization(ISO)IncomingInspectionCriteria(IIC)QualityManagementSystem(QMS)MaterialReviewBoard(MRB)CalibrationObservationOpportunityForImprovement(OFI)SupplierNonconformanceCorrectiveandPreventiveAction(CAPA)ComplaintQuarantineReworkCertificate ofConformance(CoC)PreventiveMaintenanceRiskAssessmentGoodDocumentationPractice (GDP)InternalAuditQualityPolicyNonconformingMaterialDesignTransferCritical toQuality(CTQ)TrainingFileChangeOrder(CO)SeverityExternalAuditDeviceMasterRecord(DMR)ContinuousImprovementRootCauseFood andDrugAdministration(FDA)InternationalOrganizationforStandardization(ISO)IncomingInspectionCriteria(IIC)QualityManagementSystem(QMS)MaterialReviewBoard(MRB)

Quality Week - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. Calibration
  2. Observation
  3. Opportunity For Improvement (OFI)
  4. Supplier
  5. Nonconformance
  6. Corrective and Preventive Action (CAPA)
  7. Complaint
  8. Quarantine
  9. Rework
  10. Certificate of Conformance (CoC)
  11. Preventive Maintenance
  12. Risk Assessment
  13. Good Documentation Practice (GDP)
  14. Internal Audit
  15. Quality Policy
  16. Nonconforming Material
  17. Design Transfer
  18. Critical to Quality (CTQ)
  19. Training File
  20. Change Order (CO)
  21. Severity
  22. External Audit
  23. Device Master Record (DMR)
  24. Continuous Improvement
  25. Root Cause
  26. Food and Drug Administration (FDA)
  27. International Organization for Standardization (ISO)
  28. Incoming Inspection Criteria (IIC)
  29. Quality Management System (QMS)
  30. Material Review Board (MRB)