FDA inspection
Fresenius Kabi USA, LLC: FDA inspection ending Sep 25, 2009
FDA inspection 606967 · Voluntary Action Indicated (VAI) · Lake Zurich, IL
Key facts
| Inspection ID | 606967 |
|---|---|
| Firm | Fresenius Kabi USA, LLC |
| FEI number | 3002733956 |
| Address | 3 Corporate Dr |
| City | Lake Zurich |
| State | IL |
| ZIP | 60047 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Sep 25, 2009 |
| 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