FDA Inspection 1122602 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3013625018

The FDA completed an inspection of CSL Plasma Inc. on Mar 13, 2020 in Wyoming, MI. 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
Mar 13, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wyoming, MI (United States)

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