FDA Inspection 1217198 — LFB American Plasma LLC

LFB American Plasma LLC — FEI 3014286274

The FDA completed an inspection of LFB American Plasma LLC on September 1, 2023 in High Point, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
High Point, NC (United States)