FDA Inspection 1215356 — KedPlasma, LLC
The FDA completed an inspection of KedPlasma, LLC on August 11, 2023 in Amherst, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- August 11, 2023
- Fiscal Year
- 2023
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Amherst, NY (United States)