FDA inspection

Fresenius Kabi Deutschland GmbH: FDA inspection ending Sep 5, 2019

FDA inspection 1103462 · No Action Indicated (NAI) · Friedberg (Hessen)

Key facts

Inspection ID 1103462
Firm Fresenius Kabi Deutschland GmbH
FEI number 3002851530
Address Freseniusstr. 1
City Friedberg (Hessen)
Fiscal year 2019
Inspection end date Sep 5, 2019
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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