FDA Inspection 967776 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Mar 18, 2016 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
- Mar 18, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Farmington, NM (United States)