FDA Inspection 634997 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1527870

The FDA completed an inspection of CSL Plasma Inc. on Dec 16, 2009 in Landover, MD. 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
Dec 16, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Landover, MD (United States)