FDA inspection
Versiti Wisconsin, Inc.: FDA inspection ending Nov 4, 1999
FDA inspection 3137 · Voluntary Action Indicated (VAI) · West Bend, WI
Key facts
| Inspection ID | 3137 |
|---|---|
| Firm | Versiti Wisconsin, Inc. |
| FEI number | 1000116313 |
| Address | 130 Valley Ave |
| City | West Bend |
| State | WI |
| ZIP | 53095-5314 |
| Fiscal year | 2000 |
| Inspection end date | Nov 4, 1999 |
| Classification | Voluntary Action Indicated (VAI) |
| 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