FDA inspection
BioLife Plasma Services L.P.: FDA inspection ending May 21, 2010
FDA inspection 664398 · No Action Indicated (NAI) · Cedar Rapids, IA
Key facts
| Inspection ID | 664398 |
|---|---|
| Firm | BioLife Plasma Services L.P. |
| FEI number | 1000218225 |
| Address | 5950 Rockwell Dr NE |
| City | Cedar Rapids |
| State | IA |
| ZIP | 52402 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | May 21, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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