# FDA Inspection 1258809 - KX Medical Inc - January 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/kx-medical-inc/5c12cc6b-dc01-4026-8471-2f82999b652a
Source feed: FDA_Inspections

> FDA Inspection 1258809 for KX 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: KX Medical Inc
- Inspection Date: 2025-01-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New Orleans District Office

Company: https://www.keypedia.com/companies/kx-medical-inc/b2b9b370-31ee-4cb5-b9ba-84e2d18fc62e

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea