FDA Inspection 1035181 — Actavis Laboratories UT, Inc.

Actavis Laboratories UT, Inc. — FEI 1000117147

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

Inspection Details

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

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