FDA inspection
KEDPlasma, LLC: FDA inspection ending Jan 26, 2016
FDA inspection 966746 · Voluntary Action Indicated (VAI) · Mobile, AL
Key facts
| Inspection ID | 966746 |
|---|---|
| Firm | KEDPlasma, LLC |
| FEI number | 3006210763 |
| Address | 5301 Moffett Rd |
| City | Mobile |
| State | AL |
| ZIP | 36607 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jan 26, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None 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