FDA inspection

Fresenius Kabi USA, LLC: FDA inspection ending May 4, 2012

FDA inspection 783661 · Voluntary Action Indicated (VAI) · Lake Zurich, IL

Key facts

Inspection ID 783661
Firm Fresenius Kabi USA, LLC
FEI number 3002733956
Address 3 Corporate Dr
City Lake Zurich
State IL
ZIP 60047
Country United States
Fiscal year 2012
Inspection end date May 4, 2012
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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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