FDA Inspection 944102 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3005484053

The FDA completed an inspection of CSL Plasma Inc. on September 9, 2015 in Decatur, IL. 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
September 9, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Decatur, IL (United States)