ISO-Corrective Action
ISO-Corrective Action
ISO-Corrective Action
AMENDMENT HISTORY
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1. PURPOSE:
To ensure non-conforming services are controlled to prevent them from impacting on quality and to ensure that
potential/actual problems and opportunities for improvements to processes and the overall IMS are identified and
responded.
2. SCOPE OF APPLICATION:
Applicable to the staff responsible for identifying, investigating and taking action in order to address non-
conformances, arising from internal audit, customer complaints, observations during general working practice or
product non conformance noted during inspection.
3. RESPONSIBILITY:
All Employees
Incharge - MR
4. PROCESS
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Responsibility Input Process Flow Output Document No.
Reports on
internal Identify the Nonconforming Product / Non
Incharge - MR nonconformity conformance --
Material / Service / Customer complaints
/ Customer Details
Complaints
Incharge – MR
Non
conformance Communicate to Concerned person for the
Root Cause
product / reason of non conformance and decide the --
Analysis
material / root cause of the problem
service
Incharge – MR
Corrective
Root Cause Plan and prepare a appropriate course of
Action SAL-FRM-002
Analysis action to stop the problem occurring Report
Incharge – MR
Evaluating appropriate action to prevent Corrective
Corrective
occurrence of potential nonconformities Action SAL-FRM-002
Action Report
Report
and implement the preventive action taken
Incharge – MR
Incharge – MR
Not Ok
Incharge - MR
Ok
Regularize, Do PDCA
5. Reference Documents:
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QF-SAL-002 Corrective Action Report
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