FDA inspection

Catalent Germany Eberbach GmbH: FDA inspection ending Feb 8, 2013

FDA inspection 818378 · No Action Indicated (NAI) · Eberbach

Key facts

Inspection ID 818378
Firm Catalent Germany Eberbach GmbH
FEI number 3002808098
Address Gammelsbacher Str. 2
City Eberbach
Country Germany
Fiscal year 2013
Inspection end date Feb 8, 2013
Classification No Action Indicated (NAI)
Project area Foodborne Biological Hazards
Product type Food/Cosmetics

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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