FDA inspection

Janssen Pharmaceutica, N.V.: FDA inspection ending May 14, 2014

FDA inspection 877788 · Voluntary Action Indicated (VAI) · Beerse

Key facts

Inspection ID 877788
Firm Janssen Pharmaceutica, N.V.
FEI number 3002807336
Address Turnhoutseweg 30
City Beerse
Country Belgium
Fiscal year 2014
Inspection end date May 14, 2014
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
  • 10–99 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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