FDA Inspection 1153598 — KEDPlasma LLC
The FDA completed an inspection of KEDPlasma LLC on Sep 16, 2021 in Lincoln, NE. 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
- Sep 16, 2021
- Fiscal Year
- 2021
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Lincoln, NE (United States)