Batch Manufacturing Deviation (Un-Planned) & CAPA Record





Company Name
Quality Assurance Department
Batch Manufacturing
Deviation (Un-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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