FDA inspection
Immucor GTI Diagnostics, Inc: FDA inspection ending Sep 26, 2006
FDA inspection 443786 · No Action Indicated (NAI) · Waukesha, WI
Key facts
| Inspection ID | 443786 |
|---|---|
| Firm | Immucor GTI Diagnostics, Inc |
| FEI number | 2183608 |
| Address | 20925 Crossroads Cir Ste 200 |
| City | Waukesha |
| State | WI |
| ZIP | 53186-4054 |
| Fiscal year | 2006 |
| Inspection end date | Sep 26, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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