FDA Inspection 1255230 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011083045

The FDA completed an inspection of CSL Plasma Inc. on Nov 21, 2024 in Saint Louis, MO. 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
Nov 21, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Louis, MO (United States)