FDA Inspection 1161248 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Dec 2, 2021 in Cleveland, TN. 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
- Dec 2, 2021
- Fiscal Year
- 2022
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Cleveland, TN (United States)