Ampoule / Vial /Syrup In-process Control Record




Company Name
Quality Assurance Department
  Ampoule / Vial /Syrup
In-process Control Record
Form:-
Revision No.         
Issue Date




Product:






Batch #:


Mfg. Date:




Exp. Date:

  
Sr. #
Time
pH
Volume  (ml)
Average
Volume
1
2
3
4
5
6
7
8
9
10
(ml)














































































































































                                        
           Average Volume:                                                                 Limits:


                         pH:                                                                            Limits:


Remarks:  
___________________________________________________________________

____________________________________________________________________
                                                                                                                                                                   
    Q.A Officer                                                                                              Q.A Manager


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