FDA inspection
BioLife Plasma Services L.P.: FDA inspection ending Jul 15, 2019
FDA inspection 1098038 · No Action Indicated (NAI) · Kansas City, MO
Key facts
| Inspection ID | 1098038 |
|---|---|
| Firm | BioLife Plasma Services L.P. |
| FEI number | 3014277813 |
| Address | 9500 Ne 82nd Ter |
| City | Kansas City |
| State | MO |
| ZIP | 64158 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jul 15, 2019 |
| 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
- Yes Form FDA 483 issued
- Yes 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