FDA Inspection 1145725 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3013407268

The FDA completed an inspection of CSL Plasma Inc. on Jun 4, 2021 in Indianapolis, IN. 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
Jun 4, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Indianapolis, IN (United States)

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