FDA Inspection 1131619 — KedPlasma, LLC
The FDA completed an inspection of KedPlasma, LLC on Oct 1, 2020 in Amherst, NY. 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 1, 2020
- Fiscal Year
- 2021
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Amherst, NY (United States)