FDA Inspection 1343192 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Oct 23, 2026 in Pittston, 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
- Oct 23, 2026
- Fiscal Year
- 2027
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Pittston, PA (United States)