FDA Warning Letter — LeMaitre Vascular, Inc.
The FDA took a Warning Letter action against LeMaitre Vascular, Inc. on May 11, 2010 (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
- May 11, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Center
- CDRH
- Location
- North Brunswick, NJ (United States)