# FDA Inspection 1297902 - Vortex Surgical Inc. - January 08, 2026

Source: https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/3fe96a6a-e79a-4e5d-a78d-ad9151f1c7d2
Source feed: FDA_Inspections

> FDA Inspection 1297902 for Vortex Surgical Inc. on January 08, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1297902
- Company Name: Vortex Surgical Inc.
- Inspection Date: 2026-01-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1297902 - 2026-01-08](https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/d92b6523-8057-4539-97d9-dac353add0c0)
- [FDA Inspection 1297902 - 2026-01-08](https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/bbffb154-52f5-47e4-a628-49bebda47ca4)
- [FDA Inspection 1297902 - 2026-01-08](https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/2dd0090c-2610-4309-be60-e2cd8b014887)
- [FDA Inspection 1196913 - 2023-02-09](https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/58ade412-6541-44e1-9900-33d7fadef579)
- [FDA Inspection 1196913 - 2023-02-09](https://www.keypedia.com/records/fda_inspections/vortex-surgical-inc/0aad77a1-aee0-4f89-9202-de8a4d32770a)

Company: https://www.keypedia.com/companies/vortex-surgical-inc/a846fc3d-c055-4bfe-9dc6-17229b6b775a

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