FDA inspection

Fresenius Kabi Deutschland GmbH: FDA inspection ending Sep 26, 2014

FDA inspection 900868 · Voluntary Action Indicated (VAI) · Friedberg (Hessen)

Key facts

Inspection ID 900868
Firm Fresenius Kabi Deutschland GmbH
FEI number 3002851530
Address Freseniusstr. 1
City Friedberg (Hessen)
Country Germany
Fiscal year 2014
Inspection end date Sep 26, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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