Source: FDA, document on fileFDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003194604.
Actavis Laboratories FL, Inc. dba Teva Pharmaceuticals
Davie, Florida, United States
Issue DateJuly 24, 2015
FEI Number3003194604
CountryUnited States
Status
No Warning Letter
Product Type
Drugs
Establishment Type
Pharmaceutical Manufacturer
Actavis Laboratories FL, Inc. dba Teva Pharmaceuticals FDA Form 483, Davie, Florida, July 24, 2015
