# FDA Inspection 1292268 - 3D Diagnostix Inc. - November 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/3d-diagnostix-inc/be2b4b5b-7062-4507-812b-e723ff39914e
Source feed: FDA_Inspections

> FDA Inspection 1292268 for 3D Diagnostix Inc. on November 21, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1292268
- Company Name: 3D Diagnostix Inc.
- Inspection Date: 2025-11-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1292268 - 2025-11-21](https://www.keypedia.com/records/fda_inspections/3d-diagnostix-inc/014e653c-c6e5-4fa9-a019-f1bad4a6714d)
- [FDA Inspection 1292268 - 2025-11-21](https://www.keypedia.com/records/fda_inspections/3d-diagnostix-inc/3d86e149-5a87-4874-9d27-78ecc87d771c)
- [FDA Inspection 1292268 - 2025-11-21](https://www.keypedia.com/records/fda_inspections/3d-diagnostix-inc/507873a1-0cf2-4510-8e57-def0831576c7)

Company: https://www.keypedia.com/companies/3d-diagnostix-inc/6904bc5d-6c04-4b43-8887-3cdffe87aefb

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