FDA Inspection 1079365 — KEDPlasma LLC
The FDA completed an inspection of KEDPlasma LLC on Feb 5, 2019 in Williamsville, 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
- Feb 5, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Williamsville, NY (United States)