FDA inspection

Fresenius Kabi AB: FDA inspection ending Mar 20, 2015

FDA inspection 925969 · Voluntary Action Indicated (VAI) · Uppsala

Key facts

Inspection ID 925969
Firm Fresenius Kabi AB
FEI number 3002631703
Address Rapsgatan 7
City Uppsala
Country Sweden
Fiscal year 2015
Inspection end date Mar 20, 2015
Classification Voluntary Action Indicated (VAI)
Project area Project Evaluation: Devices
Product type Devices

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
  • 10–99 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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