FDA Inspection 1053340 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1876561

The FDA completed an inspection of CSL Plasma Inc. on Apr 25, 2018 in W Lafayette, IN. 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
Apr 25, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
W Lafayette, IN (United States)