FDA Inspection 900652 — Par Pharmaceutical Inc.

Par Pharmaceutical Inc. — FEI 3008048128

The FDA completed an inspection of Par Pharmaceutical Inc. on Sep 25, 2014 in Stratford, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 25, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Stratford, CT (United States)