FDA Inspection 1061513 — Kedplasma LLC
The FDA completed an inspection of Kedplasma LLC on Jul 13, 2018 in Little Rock, 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
- Jul 13, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Little Rock, AR (United States)