FDA Inspection 1174664 — LFB USA, Inc.

LFB USA, Inc. — FEI 3013501870

The FDA completed an inspection of LFB USA, Inc. on April 8, 2022 in Charlton, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 8, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Charlton, MA (United States)