FDA inspection

Fresenius Kabi USA LLC (FK USA): FDA inspection ending Jan 26, 2009

FDA inspection 558902 · No Action Indicated (NAI) · Bensenville, IL

Key facts

Inspection ID 558902
Firm Fresenius Kabi USA LLC (FK USA)
FEI number 3007344667
Address 600 Supreme Dr
City Bensenville
State IL
ZIP 60106
Country United States
Fiscal year 2009
Inspection end date Jan 26, 2009
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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