FDA Inspection 1211512 — KEDPLASMA LLC

KEDPLASMA LLC — FEI 3013531423

The FDA completed an inspection of KEDPLASMA LLC on July 12, 2023 in Irving, TX. 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
July 12, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Irving, TX (United States)