FDA Inspection 1197658 — LFB American Plasma, LLC

LFB American Plasma, LLC — FEI 3014063934

The FDA completed an inspection of LFB American Plasma, LLC on Jan 26, 2023 in Florence, SC. 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 26, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Florence, SC (United States)

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