# FDA Inspection 1274466 - Fermatex Vascular Technologies - June 24, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/fermatex-vascular-technologies/6fd1c4f5-abce-4f3e-a235-c210f042afcf
Source feed: FDA_Inspections

> FDA Inspection 1274466 for Fermatex Vascular Technologies on June 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274466
- Company Name: Fermatex Vascular Technologies
- Inspection Date: 2025-06-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1274466 - 2025-06-24](https://www.globalkeysolutions.net/records/fda_inspections/fermatex-vascular-technologies/7e4dc6f4-6966-40da-990c-e7f6a6f4cfd7)
- [FDA Inspection 1274466 - 2025-06-24](https://www.globalkeysolutions.net/records/fda_inspections/fermatex-vascular-technologies/6cd8d154-0301-48f5-900f-e8bdd8af2490)
- [FDA Inspection 1274466 - 2025-06-24](https://www.globalkeysolutions.net/records/fda_inspections/fermatex-vascular-technologies/214d7657-1b8a-4cf8-b84c-0e16afc50384)

Company: https://www.globalkeysolutions.net/companies/fermatex-vascular-technologies/42ee7a5f-736d-45ae-a63a-fadb8ecd7a61

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7