FDA inspection
KEDPlasma LLC: FDA inspection ending Oct 10, 2025
FDA inspection 1283322 · No Action Indicated (NAI) · Lincoln, NE
Key facts
| Inspection ID | 1283322 |
|---|---|
| Firm | KEDPlasma LLC |
| FEI number | 1720702 |
| Address | 733 N 45th St |
| City | Lincoln |
| State | NE |
| ZIP | 68503 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Oct 10, 2025 |
| 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