FDA Inspection 1046450 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on Mar 9, 2018 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
- Mar 9, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Greenville, NC (United States)