FDA Inspection 829594 — Actavis Incorporated

Actavis Incorporated — FEI 1419832

The FDA completed an inspection of Actavis Incorporated on Apr 30, 2013 in Mt Prospect, IL. 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
Apr 30, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mt Prospect, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.