FDA Inspection 587317 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1000307513

The FDA completed an inspection of CSL Plasma Inc. on May 22, 2009 in Knoxville, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 22, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Knoxville, TN (United States)