Batch Manufacturing Deviation (Planned) & CAPA Record

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