FDA Inspection 1194233 — KEDPLASMA LLC
The FDA completed an inspection of KEDPLASMA LLC on Dec 8, 2022 in Pittston, PA. 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 8, 2022
- Fiscal Year
- 2023
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Pittston, PA (United States)