# FDA Inspection 1288394 - Koya Medical, Inc - October 24, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/koya-medical-inc/0870bcc8-5c05-47d0-8a3e-03f384f21769
Source feed: FDA_Inspections

> FDA Inspection 1288394 for Koya Medical, Inc on October 24, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288394
- Company Name: Koya Medical, Inc
- Inspection Date: 2025-10-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Dallas District Office

## Related Documents

- [FDA Inspection 1288394 - 2025-10-24](https://www.globalkeysolutions.net/records/fda_inspections/koya-medical-inc/e147fc28-f2cc-40ea-bb86-bcaffc6b8e30)
- [FDA Inspection 1288394 - 2025-10-24](https://www.globalkeysolutions.net/records/fda_inspections/koya-medical-inc/96fca4fb-8e34-4540-853e-3ca58a798858)
- [FDA Inspection 1288394 - 2025-10-24](https://www.globalkeysolutions.net/records/fda_inspections/koya-medical-inc/e584d88e-66df-42ee-8d9e-5d004bbf80cc)

Company: https://www.globalkeysolutions.net/companies/koya-medical-inc/946d648a-9b96-43b9-b8ee-2f88671fc4a6

Office: https://www.globalkeysolutions.net/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9