FDA Inspection 952587 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1930460

The FDA completed an inspection of CSL Plasma Inc. on December 15, 2015 in Kansas City, 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
December 15, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kansas City, MO (United States)