FDA Inspection 1160366 — CSL Plasma, Inc.

CSL Plasma, Inc. — FEI 3017502454

The FDA completed an inspection of CSL Plasma, Inc. on Dec 16, 2021 in Allentown, PA. 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
Dec 16, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Allentown, PA (United States)

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