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Question:

Audit evidence may be obtained from people, processes, equipment, tools, materials, documentation and by observation and, is defined as records, statements of facts or other information which are relevant to the audit criteria and verifiable. (ISO 19011:2018):
  1. True
  2. False






Q2. The process of determining whether the corrective action requested has been implemented is called the follow-up. This can be done by reviewing documentation submitted by the client or by visiting the client premises:

  1. True
  2. False
Correct Answer

Q3. Rapid cooling is an example of...

  1. a corrective action
  2. a hazard
  3. a critical limit
  4. a control measure
  5. Incorrect monitoring
Correct Answer

Q4. The organisation shall ensure that finished products are labelled according to all applicable food safety regulatory requirements in the country of manufacturing:

  1. True
  2. False
Correct Answer

Q5. Any ‘close out’ of a corrective action must be completed by the auditor attending the client premises where the initial audit took place and the CAR was raised:

  1. True
  2. False
Correct Answer

Q6. Minor NC should be closed out and the objective evidence should be submitted to the CB:

  1. within 14 days
  2. within 28 days
  3. within 90 days
  4. Incorrect in the next audit visit
Correct Answer

Q7. An audit by the organisation of its own management system and procedures is also known as a:

  1. First party audit
  2. Second party audit
  3. Third party audit
  4. Surveillance audit
Correct Answer

Q8. Which of the following clauses are NOT part of BRC? i) Product safety & quality management ii) Continual improvement iii) Product inspection & testing iv) Operation

  1. i & iv
  2. ii & iv
  3. i, ii & iii
  4. All of the answers
Correct Answer

Q9. What does HACCP stand for?

  1. Hazard Analysis and Critical Control Point
  2. Hazard And Critical Control Point
  3. Health Analysis and Critical Control Point
  4. Hazard And Critical Cooking Point
Correct Answer

Q10. Which of the listed document types ARE required GMP documentation?

  1. Site Master File and Specifications
  2. Manufacturing Formulae, Processing, Packaging and Testing Instructions
  3. Certificate of Analysis, Procedures and Protocols
  4. Technical Agreements, Records and Reports
  5. All of the above
Correct Answer










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