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FDA Inspection 682802 — LeMaitre Vascular, Inc.

LeMaitre Vascular, Inc. — FEI 1220948

The FDA completed an inspection of LeMaitre Vascular, Inc. on September 22, 2010 in Burlington, MA. 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
September 22, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Burlington, MA (United States)

Facility

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FDA data resources