FDA Inspection 1215553 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3013403342

The FDA completed an inspection of CSL Plasma Inc. on Jul 13, 2023 in Saint Paul, MN. 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
Jul 13, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saint Paul, MN (United States)

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