FDA inspection

Organon Pharma (UK) Ltd.: FDA inspection ending Mar 9, 2010

FDA inspection 651971 · No Action Indicated (NAI) · Cramlington

Key facts

Inspection ID 651971
Firm Organon Pharma (UK) Ltd.
FEI number 3002807653
Address Shotton Lane
City Cramlington
Country United Kingdom
Fiscal year 2010
Inspection end date Mar 9, 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
  • 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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