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FDA Inspection
•LeMaitre Vascular, Inc.•August 27, 2020

LeMaitre Vascular, Inc. – FDA Inspection, Aug 27, 2020

Record Details

This FDA Inspection record concerns LeMaitre Vascular, Inc., with an inspection on August 27, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company
LeMaitre Vascular, Inc.
Inspection Date
August 27, 2020
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 2c1189c4-a231-4cc3-8013-740f42ba51c2

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1129204
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of LeMaitre Vascular, Inc.

10
DateClassificationOfficeProject area
May 16, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
June 15, 2022VAICenter for Devices and Radiological HealthCompliance: Devices
July 26, 2021NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
August 1, 2017NAICenter for Devices and Radiological HealthCompliance: Devices
March 4, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
View all 10 other inspections on the company page
Other documents for LeMaitre Vascular, Inc.
  • FDA Inspection 1206543 - 2023-05-16
  • FDA Inspection 1172108 - 2022-06-15
  • FDA Inspection 1148251 - 2021-07-26
  • FDA Inspection 1023176 - 2017-08-01
  • FDA Inspection 823948 - 2013-03-04

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