FDA Inspection 1044857 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Dec 21, 2017 in Shreveport, LA. 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
- Dec 21, 2017
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Shreveport, LA (United States)