FDA inspection
CSL Plasma Inc.: FDA inspection ending Feb 12, 2020
FDA inspection 1117599 · Voluntary Action Indicated (VAI) · New Hope, MN
Key facts
| Inspection ID | 1117599 |
|---|---|
| Firm | CSL Plasma Inc. |
| FEI number | 3012796872 |
| Address | 4401 Winnetka Ave N |
| City | New Hope |
| State | MN |
| ZIP | 55428 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Feb 12, 2020 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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