FDA inspection

Johnson & Johnson Pharmaceutical Research & Development, LLC: FDA inspection ending Mar 24, 2009

FDA inspection 573200 · No Action Indicated (NAI) · Raritan, NJ

Key facts

Inspection ID 573200
Firm Johnson & Johnson Pharmaceutical Research & Development, LLC
FEI number 3006192174
Address 920 U.S. Highway 202, P.O. Box 300
City Raritan
State NJ
ZIP 08869
Country United States
Fiscal year 2009
Inspection end date Mar 24, 2009
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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