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FDA Inspection 915471 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1978037

The FDA completed an inspection of CSL Plasma Inc. on February 13, 2015 in Omaha, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 13, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Omaha, NE (United States)

Facility

Other inspections at this facility

  • 1150540 (NAI Wed Aug 04 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1018616 (NAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 822927 (NAI Fri Mar 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 745538 (NAI Thu Sep 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 605487 (VAI Fri Aug 14 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources