FDA Inspection 826757 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on Apr 3, 2013 in Greenville, NC. 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
- Apr 3, 2013
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Greenville, NC (United States)