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FDA Inspection 1035181 — Actavis Laboratories UT, Inc.

Actavis Laboratories UT, Inc. — FEI 1000117147

The FDA completed an inspection of Actavis Laboratories UT, Inc. on October 25, 2017 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 25, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salt Lake City, UT (United States)

Facility

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