FDA Inspection 1148848 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3012796872

The FDA completed an inspection of CSL Plasma Inc. on Aug 3, 2021 in New Hope, 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
Aug 3, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Blood and Blood Products
Location
New Hope, MN (United States)

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