FDA Inspection 1148557 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3013158871

The FDA completed an inspection of CSL Plasma Inc. on Aug 12, 2021 in Port Arthur, TX. 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
Aug 12, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Port Arthur, TX (United States)

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