Dear all,
Can anyone help me on corrective action during process?
When QC inspector found problem/deviation during process, where should they recorded the deviation and corrective action? Should we develop a new form or we make a new column for deviation and corrective action in QC process record?
For example, when seamer is out of spec.,QC will inform production to stop the line and notify the QA Manager/Supervisor. Hold and segregate the FG. Maintenance will adjust the seamer and QC shall check the seamer before start the production again. This is a immediate corrective action? Can maintenance, production and QC sign and verify in 1 form? How?
Does anyone have the example for this problem?
TQ
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