FDA inspection

N.V. Organon: FDA inspection ending Sep 7, 2017

FDA inspection 1031159 · Voluntary Action Indicated (VAI) · Oss

Key facts

Inspection ID 1031159
Firm N.V. Organon
FEI number 3002806821
Address Kloosterstraat 6
City Oss
Country Netherlands
Fiscal year 2017
Inspection end date Sep 7, 2017
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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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