FDA inspection
Octapharma Plasma, Inc.: FDA inspection ending Apr 25, 2014
FDA inspection 881205 · No Action Indicated (NAI) · North Little Rock, AR
Key facts
| Inspection ID | 881205 |
|---|---|
| Firm | Octapharma Plasma, Inc. |
| FEI number | 3007960042 |
| Address | 5121 Warden Rd Ste B |
| City | North Little Rock |
| State | AR |
| ZIP | 72116 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Apr 25, 2014 |
| 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
- 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