# FDA Inspection 1293356 - Focalyx Technologies - December 01, 2025

Source: https://www.keypedia.com/records/fda_inspections/focalyx-technologies/13df75f7-4a6a-47d2-bf49-8198a35f839e
Source feed: FDA_Inspections

> FDA Inspection 1293356 for Focalyx Technologies on December 01, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1293356
- Company Name: Focalyx Technologies
- Inspection Date: 2025-12-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1293356 - 2025-12-01](https://www.keypedia.com/records/fda_inspections/focalyx-technologies/5204e94d-234d-4a54-a649-c071533cf246)
- [FDA Inspection 1293356 - 2025-12-01](https://www.keypedia.com/records/fda_inspections/focalyx-technologies/266e3872-b1ca-4ec1-8743-c509e08ab7d4)
- [FDA Inspection 1293356 - 2025-12-01](https://www.keypedia.com/records/fda_inspections/focalyx-technologies/97a8f826-1378-49b1-840f-16870b94f264)
- [FDA Inspection 1220060 - 2023-08-14](https://www.keypedia.com/records/fda_inspections/focalyx-technologies/cb782ae9-0ca0-4696-abf4-572c6399908d)
- [FDA Inspection 1220060 - 2023-08-14](https://www.keypedia.com/records/fda_inspections/focalyx-technologies/f1195d5f-b9bf-42b0-94be-47768edd480f)

Company: https://www.keypedia.com/companies/focalyx-technologies/fe709d40-ab14-4517-92ea-5dd88985ab6a

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