FDA Inspection 650747 — Actavis Totowa LLC

Actavis Totowa LLC — FEI 3005788029

The FDA completed an inspection of Actavis Totowa LLC on Feb 3, 2010 in Totowa, NJ. 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
Feb 3, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Totowa, NJ (United States)

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