# FDA Inspection 1258809 - KFx Medical, Inc. - January 21, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/kfx-medical-inc/ff2146b8-d9f3-4481-9296-45e06cad0172/
Source feed: FDA_Inspections

> FDA Inspection 1258809 for KFx Medical, Inc. on January 21, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258809
- Company Name: KFx Medical, Inc.
- Inspection Date: 2025-01-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 872299 - 2014-03-31](https://www.globalkeysolutions.net/api/records/fda_inspections/kfx-medical-inc/ec649846-cb56-451f-91ba-f76c8c8d3701/)
- [FDA Inspection 872299 - 2014-03-31](https://www.globalkeysolutions.net/api/records/fda_inspections/kfx-medical-inc/bf0e45ae-d07a-4514-aa05-6b13cf683b71/)

Company: https://www.globalkeysolutions.net/companies/kfx-medical-inc/9876b099-37b9-444b-88f3-a6b6bba435be

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