Company Name
|
Quality Assurance Department
|
Batch Manufacturing
Deviation (Planned) & CAPA Record
|
Form No.
|
Issue Date:
|
|
Revision No:
|
Product Name:
__________________ Batch No.:
__________________
Mfg. Date: _____________________ Exp. Date: __________________
Sr.No.
|
Date
|
Deviation
Number
|
Deviations
Observed and its CAPA (if any)
|
Remarks
|
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