FDA Inspection 1205390 — KEDPLASMA LLC

KEDPLASMA LLC — FEI 3018002105

The FDA completed an inspection of KEDPLASMA LLC on April 6, 2023 in Hendersonville, NC. 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
April 6, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Hendersonville, NC (United States)