# FDA Inspection 1288366 - Homtex Inc - October 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/homtex-inc/35bafdb5-3582-4e51-a133-ec6bce3b5fb1
Source feed: FDA_Inspections

> FDA Inspection 1288366 for Homtex Inc on October 16, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288366
- Company Name: Homtex Inc
- Inspection Date: 2025-10-16
- 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 1288366 - 2025-10-16](https://www.keypedia.com/records/fda_inspections/homtex-inc/9935b846-3e67-4251-9eba-57d90e752ff0)
- [FDA Inspection 1288366 - 2025-10-16](https://www.keypedia.com/records/fda_inspections/homtex-inc/357386d2-cd0f-45fe-ad1d-3d81ebf8c2fa)
- [FDA Inspection 1288366 - 2025-10-16](https://www.keypedia.com/records/fda_inspections/homtex-inc/fdcc53a3-18c6-47fb-9b19-35b1bfc17f40)

Company: https://www.keypedia.com/companies/homtex-inc/ba2e0ff4-48b0-4c32-bfac-e105288cd746

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