FDA Inspection 982045 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1978022

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