FDA Inspection 809838 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on Nov 15, 2012 in Hot Springs, AR. 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 15, 2012
- Fiscal Year
- 2013
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Hot Springs, AR (United States)