Company Name
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Quality Assurance Department
|
|
Ampoule / Vial /Syrup
In-process Control Record
|
Form:-
|
|
Revision No.
Issue
Date
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||
Product:
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Batch #:
|
Mfg. Date:
|
Exp. Date:
|
Sr. #
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Time
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pH
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Volume
(ml)
|
Average
Volume
|
|||||||||
1
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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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