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FDA Inspection 1150667 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 2176201

The FDA completed an inspection of CSL Plasma Inc. on August 19, 2021 in Duluth, MN. 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
August 19, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Duluth, MN (United States)

Facility

Other inspections at this facility

  • 1010194 (NAI Fri Apr 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919564 (NAI Fri Mar 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810850 (NAI Thu Dec 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 730727 (NAI Wed Jun 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 580987 (VAI Thu Apr 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources