FDA inspection
Immucor GTI Diagnostics, Inc: FDA inspection ending Jan 13, 2010
FDA inspection 639478 · Voluntary Action Indicated (VAI) · Waukesha, WI
Key facts
| Inspection ID | 639478 |
|---|---|
| Firm | Immucor GTI Diagnostics, Inc |
| FEI number | 2183608 |
| Address | 20925 Crossroads Cir Ste 200 |
| City | Waukesha |
| State | WI |
| ZIP | 53186 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jan 13, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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