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FDA Inspection 864480 — Actavis Laboratories FL, Inc.

Actavis Laboratories FL, Inc. — FEI 3003194604

The FDA completed an inspection of Actavis Laboratories FL, Inc. on December 20, 2013 in Davie, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 20, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Davie, FL (United States)

Facility

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  • 1115283 (OAI Fri Jan 17 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1059371 (OAI Thu Jul 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1033875 (VAI Tue Nov 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources