FDA Inspection 1016456 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011511768

The FDA completed an inspection of CSL Plasma Inc. on Jun 14, 2017 in Glen Burnie, MD. 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 14, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Glen Burnie, MD (United States)

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