FDA Inspection 1090777 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3010606902

The FDA completed an inspection of CSL Plasma Inc. on May 13, 2019 in Saint Louis, MO. 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 13, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Louis, MO (United States)