FDA Inspection 783911 — Actavis South Atlantic LLC

Actavis South Atlantic LLC — FEI 3004090892

The FDA completed an inspection of Actavis South Atlantic LLC on Apr 25, 2012 in Sunrise, FL. 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 25, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sunrise, FL (United States)

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