FDA Inspection 1067753 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Sep 20, 2018 in Farmington, NM. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 20, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Farmington, NM (United States)