FDA inspection
BPL Plasma, Inc.: FDA inspection ending Dec 8, 1999
FDA inspection 9800 · No Action Indicated (NAI) · Houston, TX
Key facts
| Inspection ID | 9800 |
|---|---|
| Firm | BPL Plasma, Inc. |
| FEI number | 2177765 |
| Address | 5202 Aldine Mail Route Rd |
| City | Houston |
| State | TX |
| ZIP | 77039-3804 |
| Fiscal year | 2000 |
| Inspection end date | Dec 8, 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