FDA Inspection 889051 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1930460

The FDA completed an inspection of CSL Plasma Inc. on Jul 23, 2014 in Kansas City, MO. 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
Jul 23, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kansas City, MO (United States)

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