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Aplicare Products, LLC 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 1220701.

Aplicare Products, LLC

Meriden, Connecticut, United States
Issue DateJanuary 15, 2016
FEI Number1220701
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Aplicare Products, LLC FDA Form 483, Meriden, Connecticut, January 15, 2016