FDA inspection

Orgapharm: FDA inspection ending Apr 9, 2014

FDA inspection 876642 · Voluntary Action Indicated (VAI) · Pithiviers

Key facts

Inspection ID 876642
Firm Orgapharm
FEI number 3002807503
Address Rue Du Moulin De La Canne
City Pithiviers
Country France
Fiscal year 2014
Inspection end date Apr 9, 2014
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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