FDA Inspection 1033874 — Actavis Laboratories FL, Inc.

Actavis Laboratories FL, Inc. — FEI 3003937591

The FDA completed an inspection of Actavis Laboratories FL, Inc. on Dec 1, 2017 in Sunrise, FL. 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
Dec 1, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sunrise, FL (United States)

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