FDA inspection
CSL Plasma Inc.: FDA inspection ending Dec 13, 2012
FDA inspection 810850 · No Action Indicated (NAI) · Duluth, MN
Key facts
| Inspection ID | 810850 |
|---|---|
| Firm | CSL Plasma Inc. |
| FEI number | 2176201 |
| Address | 106 W Superior St |
| City | Duluth |
| State | MN |
| ZIP | 55802 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Dec 13, 2012 |
| 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