FDA Inspection 822927 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1978037

The FDA completed an inspection of CSL Plasma Inc. on March 15, 2013 in Omaha, NE. 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
March 15, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Omaha, NE (United States)