FDA Inspection 1114206 — KEDPlasma LLC
The FDA completed an inspection of KEDPlasma LLC on Nov 14, 2019 in Tucker, GA. 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
- Nov 14, 2019
- Fiscal Year
- 2020
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Tucker, GA (United States)