FDA inspection

Catalent Germany Eberbach GmbH: FDA inspection ending Mar 5, 2010

FDA inspection 654570 · Voluntary Action Indicated (VAI) · Eberbach

Key facts

Inspection ID 654570
Firm Catalent Germany Eberbach GmbH
FEI number 3002808098
Address Gammelsbacher Str. 2
City Eberbach
Country Germany
Fiscal year 2010
Inspection end date Mar 5, 2010
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
  • 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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