FDA Inspection 1167906 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Mar 10, 2022 in Port Orange, FL. 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
- Mar 10, 2022
- Fiscal Year
- 2022
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Port Orange, FL (United States)