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FDA Inspection 1129204 — LeMaitre Vascular, Inc.

LeMaitre Vascular, Inc. — FEI 1220948

The FDA completed an inspection of LeMaitre Vascular, Inc. on August 27, 2020 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
August 27, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Burlington, MA (United States)

Facility

Other inspections at this facility

  • 1206543 (VAI Tue May 16 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1172108 (VAI Wed Jun 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1148251 (NAI Mon Jul 26 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1023176 (NAI Tue Aug 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 823948 (VAI Mon Mar 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources