FDA Inspection 1319396 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on May 21, 2026 in Altoona, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 21, 2026
- Fiscal Year
- 2026
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Altoona, PA (United States)