FDA Inspection 1040020 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3010375375

The FDA completed an inspection of CSL Plasma Inc. on Jan 4, 2018 in Dallas, 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
Jan 4, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dallas, TX (United States)

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