FDA Inspection 961394 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011083045

The FDA completed an inspection of CSL Plasma Inc. on Feb 23, 2016 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
Feb 23, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Louis, MO (United States)