FDA Inspection 1193907 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1641185

The FDA completed an inspection of CSL Plasma Inc. on December 9, 2022 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
December 9, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Tulsa, OK (United States)