FDA inspection

Actavis LLC: FDA inspection ending Aug 8, 2019

FDA inspection 1100659 · No Action Indicated (NAI) · Edison, NJ

Key facts

Inspection ID 1100659
Firm Actavis LLC
FEI number 3009017204
Address 47 Brunswick Ave
City Edison
State NJ
ZIP 08817
Country United States
Fiscal year 2019
Inspection end date Aug 8, 2019
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

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