STERIS CPO Quality Month

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Across
  1. 1. Good Documentation Practices
  2. 3. immediate action taken to reduce or eliminate further impact on product
  3. 7. failure of a device to meet its performance specifications or otherwise perform as intended
  4. 9. Good Manufacturing Practices
  5. 11. a non-fulfillment of a specified requirement
  6. 14. the verification and adjustment of measuring equipment to agree with a known standard, within a specified accuracy
  7. 15. any written or electronic documentation providing evidence that activities were performed, and their results
  8. 16. communication that alleges deficiencies of a device released for distribution
Down
  1. 2. a shortcoming or imperfection
  2. 4. preventative measures put in place to detect potential defects in manufactured products or services before they reach customers
  3. 5. the degree of conformity of a measure to a standard or true value
  4. 6. Quality Management System
  5. 8. the permissible range of variation of a characteristic from its nominal value
  6. 10. Quality System Element
  7. 12. action taken on a nonconforming product so that it will fulfill the specified requirements before it is released for distribution
  8. 13. action taken to eliminate a detected nonconformity