FDA Inspection 1210801 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on May 24, 2023 in Anderson, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- May 24, 2023
- Fiscal Year
- 2023
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Anderson, SC (United States)