FDA Inspection 810914 — Actavis Laboratories UT, Inc.

Actavis Laboratories UT, Inc. — FEI 1000117147

The FDA completed an inspection of Actavis Laboratories UT, Inc. on December 14, 2012 in Salt Lake City, UT. 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 14, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salt Lake City, UT (United States)