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