1. Control of documents
2. Control of records
3. Control of Production Equipment, tools and CNC programs
4. Control of Non conforming products
5. Preventive Action
6. Corrective Action

1. Control of Non Confirmative Output

2. Identifying the root cause for Non confirmative and corrective action plan.

3. Control product's quality w.r.t the related codes.

4. Control of records.

5. Preparation of q m s and implementation

1. Control of documents (4.2.3)
2. Control of records (4.2.4)
3. Internal Audit (8.2.2)
4. Control of Non conforming products (8.3)
6. Corrective Action (8.5.2)
7. Preventive Action (8.5.3)

If you have the better answer, then send it to us. We will display your answer after the approval.
Rules to Post Answers in CoolInterview.com:-

There should not be any Spelling Mistakes.

There should not be any Gramatical Errors.

Answers must not contain any bad words.

Answers should not be the repeat of same answer, already approved.

Answer should be complete in itself.

Name :*
Email Id :*
Answer :*
Verification Code	Not readable? Load New Code
Enter the above shown code:*
	Inform me about updated answers to this question