FDA inspection
Versiti Illinois, Inc.: FDA inspection ending Dec 12, 2008
FDA inspection 557351 · No Action Indicated (NAI) · Elgin, IL
Key facts
| Inspection ID | 557351 |
|---|---|
| Firm | Versiti Illinois, Inc. |
| FEI number | 1471716 |
| Address | 1140 N Mclean Blvd Ste 1140-D |
| City | Elgin |
| State | IL |
| ZIP | 60123 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Dec 12, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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