FDA inspection

Actavis LLC: FDA inspection ending Jul 7, 2016

FDA inspection 978483 · Voluntary Action Indicated (VAI) · Edison, NJ

Key facts

Inspection ID 978483
Firm Actavis LLC
FEI number 3009017204
Address 47 Brunswick Ave
City Edison
State NJ
ZIP 08817
Country United States
Fiscal year 2016
Inspection end date Jul 7, 2016
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections