# FDA Inspection 1302468 - DiFusion Technologies - February 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/difusion-technologies/06f8beeb-e440-4129-a95b-e7e23e4c1c36
Source feed: FDA_Inspections

> FDA Inspection 1302468 for DiFusion Technologies on February 12, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1302468
- Company Name: DiFusion Technologies
- Inspection Date: 2026-02-12
- 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 1302468 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/difusion-technologies/75788dad-b328-43fe-85ca-4feba4136524)
- [FDA Inspection 1302468 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/difusion-technologies/422f60d6-7b37-447f-af28-f3b9f3207ae3)
- [FDA Inspection 1302468 - 2026-02-12](https://www.keypedia.com/records/fda_inspections/difusion-technologies/b4edda52-416f-4d4e-94c3-5394d6a125a8)

Company: https://www.keypedia.com/companies/difusion-technologies/c939cd95-299e-48a9-8a66-6aacb5396d95

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