FDA inspection
Innovative Blood Resources: FDA inspection ending Oct 27, 1999
FDA inspection 2548 · No Action Indicated (NAI) · Minneapolis, MN
Key facts
| Inspection ID | 2548 |
|---|---|
| Firm | Innovative Blood Resources |
| FEI number | 1000221043 |
| Address | 3200 Main St Nw Ste 120 |
| City | Minneapolis |
| State | MN |
| ZIP | 55448-1161 |
| Fiscal year | 2000 |
| Inspection end date | Oct 27, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood & Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None 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