FDA Inspection 1180659 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Sep 30, 2022 in Cleveland, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 30, 2022
- Fiscal Year
- 2022
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Cleveland, OH (United States)