# FDA Inspection 1289384 - Vesalio - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/vesalio/0aacad09-616f-4acb-8d63-983a9919a080
Source feed: FDA_Inspections

> FDA Inspection 1289384 for Vesalio on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1289384
- Company Name: Vesalio
- Inspection Date: 2025-10-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1289384 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/vesalio/8045eb98-b164-46f4-aaf8-82f768c81e20)
- [FDA Inspection 1289384 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/vesalio/a1f557dc-d808-433b-85a3-fd43538e8acc)
- [FDA Inspection 1289384 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/vesalio/895cb0c0-fda5-40f6-b098-5fd2abd2ad5b)
- [FDA Inspection 1169404 - 2022-05-05](https://www.keypedia.com/records/fda_inspections/vesalio/76efbc79-b117-4493-9a85-40977718b884)

Company: https://www.keypedia.com/companies/vesalio/cabeb545-6556-41c3-a723-c7fe7389acd9

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