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FDA Inspection 610607 — Actavis Laboratories FL, Inc.

Actavis Laboratories FL, Inc. — FEI 3003194604

The FDA completed an inspection of Actavis Laboratories FL, Inc. on September 4, 2009 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
September 4, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Davie, FL (United States)

Facility

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Recent compliance actions

FDA data resources