FDA Inspection 1329850 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3015745056

The FDA completed an inspection of CSL Plasma Inc. on Jul 31, 2026 in Clifton, NJ. 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 31, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Clifton, NJ (United States)

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