FDA Inspection 685143 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1930460

The FDA completed an inspection of CSL Plasma Inc. on Sep 27, 2010 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
Sep 27, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kansas City, MO (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.