FDA inspection
Csl Plasma, Inc.: FDA inspection ending Nov 22, 1999
FDA inspection 5827 · Voluntary Action Indicated (VAI) · Minneapolis, MN
Key facts
| Inspection ID | 5827 |
|---|---|
| Firm | Csl Plasma, Inc. |
| FEI number | 2177738 |
| Address | 304 E Lake St |
| City | Minneapolis |
| State | MN |
| ZIP | 55408-2453 |
| Fiscal year | 2000 |
| Inspection end date | Nov 22, 1999 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood & Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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