FDA inspection
Versiti Illinois Inc: FDA inspection ending Oct 1, 1999
FDA inspection 1111 · Aurora, IL
Key facts
| Inspection ID | 1111 |
|---|---|
| Firm | Versiti Illinois Inc |
| FEI number | 1470274 |
| Address | 1200 N Highland Ave |
| City | Aurora |
| State | IL |
| ZIP | 60506-1401 |
| Fiscal year | 2000 |
| Inspection end date | Oct 1, 1999 |
| Project area | Blood & Blood Products |
| Product type | Biologics |
At a glance
- None 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