Source: FDA, document on file. FDA 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3003194604.
Observations9
Issue DateJuly 24, 2015
StatusNo Warning Letter
Establishment TypePharmaceutical Manufacturer
Related Inspections9
Establishment Details
Firm
Actavis Laboratories FL, Inc. dba Teva Pharmaceuticals
Issued To
Andrx Pharmaceuticals, Inc
Location
Davie, Florida, United States
FEI Number
3003194604
Establishment Type
Pharmaceutical Manufacturer
Product Type
Drugs
Issue Date
July 24, 2015
Country
United States
Inspection History, 2009 to 2025
VAI7
OAI2
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.