FDA inspection
Versiti Indiana, Inc.: FDA inspection ending Sep 18, 2012
FDA inspection 799301 · Voluntary Action Indicated (VAI) · Lafayette, IN
Key facts
| Inspection ID | 799301 |
|---|---|
| Firm | Versiti Indiana, Inc. |
| FEI number | 1828129 |
| Address | 2200 Elmwood Ave Ste D16 |
| City | Lafayette |
| State | IN |
| ZIP | 47904 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Sep 18, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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
- 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