FDA inspection
Octapharma Plasma, Inc.: FDA inspection ending Oct 24, 2019
FDA inspection 1107384 · Voluntary Action Indicated (VAI) · Orlando, FL
Key facts
| Inspection ID | 1107384 |
|---|---|
| Firm | Octapharma Plasma, Inc. |
| FEI number | 3012544735 |
| Address | 5739B Edgewater Dr |
| City | Orlando |
| State | FL |
| ZIP | 32810 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Oct 24, 2019 |
| 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
- 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