FDA inspection
Oklahoma Blood Institute - IRB: FDA inspection ending Aug 29, 2003
FDA inspection 288528 · Voluntary Action Indicated (VAI) · Oklahoma City, OK
Key facts
| Inspection ID | 288528 |
|---|---|
| Firm | Oklahoma Blood Institute - IRB |
| FEI number | 1641554 |
| Address | 1001 N Lincoln Blvd |
| City | Oklahoma City |
| State | OK |
| ZIP | 73104-3251 |
| Fiscal year | 2003 |
| Inspection end date | Aug 29, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None 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