FDA Inspection
LeMaitre Vascular, Inc.LeMaitre Vascular, Inc. – FDA Inspection, Oct 31, 2012
Record Details
This FDA Inspection record concerns LeMaitre Vascular, Inc., with an inspection on October 31, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LeMaitre Vascular, Inc.
- Inspection Date
- October 31, 2012
- Product Type
- Devices
View Company Profile
ID · c6d41af7-ee35-48f2-ba58-058f1dd022a9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 808236
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of LeMaitre Vascular, Inc.
10| Date | Classification | Office | Project area |
|---|---|---|---|
| May 16, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 15, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 26, 2021 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| August 27, 2020 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 1, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
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