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Accupack Midwest Inc Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 1000122754.

Accupack Midwest Inc

Cincinnati, Ohio, United States
Issue DateOctober 11, 2012
FEI Number1000122754
CountryUnited States
Status
1 Related Warning Letter
Product Type
Drugs
Accupack Midwest Inc FDA Form 483, Cincinnati, Ohio, October 11, 2012