FDA inspection

Janssen Pharmaceutica N.V.: FDA inspection ending Dec 10, 2010

FDA inspection 704229 · No Action Indicated (NAI) · Geel

Key facts

Inspection ID 704229
Firm Janssen Pharmaceutica N.V.
FEI number 3002807337
Address Janssen-Pharmaceuticalaan 3
City Geel
Country Belgium
Fiscal year 2011
Inspection end date Dec 10, 2010
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
  • 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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