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FDA Inspection 740404 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1672443

The FDA completed an inspection of CSL Plasma Inc. on August 18, 2011 in Tulsa, OK. 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 18, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tulsa, OK (United States)

Facility

Other inspections at this facility

  • 1193274 (NAI Thu Dec 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1028948 (VAI Fri Sep 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928921 (NAI Wed May 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 834501 (NAI Tue Jun 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources