FDA Inspection 1044392 — LeMaitre Vascular, Inc.

LeMaitre Vascular, Inc. — FEI 1000121696

The FDA completed an inspection of LeMaitre Vascular, Inc. on February 16, 2018 in North Brunswick, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 16, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
North Brunswick, NJ (United States)