FDA inspection

Catalent France Beinheim SA: FDA inspection ending Mar 20, 2014

FDA inspection 878382 · No Action Indicated (NAI) · Beinheim

Key facts

Inspection ID 878382
Firm Catalent France Beinheim SA
FEI number 3002808036
Address 74 Rue Principale
City Beinheim
Country France
Fiscal year 2014
Inspection end date Mar 20, 2014
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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