FDA Warning Letter — LeMaitre Vascular, Inc.

Case 713502 — FEI 1000121696

The FDA took a Warning Letter action against LeMaitre Vascular, Inc. on Aug 11, 2025 (North Brunswick, NJ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
LeMaitre Vascular, Inc.
Date
Aug 11, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
North Brunswick, NJ (United States)

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