Documente Academic
Documente Profesional
Documente Cultură
QUALITY
PROCEDURE
Purpose
This procedure is to assure that the nonconformity is followed up as the required
II.
method.
Scope
All of the process, products, and quality that are inappropriate or potentially to non-
III.
conformity.
Responsibility
III.1
Quality Assurance section shall be responsible to follow up the corrective
and preventive action request.
III.2
Aftersales Service section shall be responsible for following up and
ensuring the corrective and preventive action to the customer complaint.
III.3
Related work unit shall be responsible for following up the corrective and
preventive action request, audit findings, non conforming report, and customer
complaint.
III.4
All personnel shall be responsible to propose the corrective and preventive
IV.
V.
Related Document
5.1. Quality Manual Measuring, Analysis, Improvement (MM-8)
5.2. Quality Procedure Record Control (PM-4.02)
5.3. Quality Procedure Monitoring Customer Complaint Method (PM-8.01)
5.4. Quality Procedure Internal Audit (PM-8.02)
5.5. Quality Procedure Non-conforming Product Control (PM-8.06)
VI.
Attachment
6.1. NCR Product (Form No.: IV-01.012)
6.2. Corrective and Preventive Action Request (Form No. : IV- 01.014)
6.3. NCR Audit Internal (Form No. IV-01.016
6.4. Non conforming Investigation and Corrective Analysis (Form No.: IV-01.032)
6.5. Customer Complaint (Form No. : IV-01.084).
Prepared by:
ISO Team
Checked by:
Management Representative
Approved by:
President Director
Agus Purwantono
Roos Diatmoko