# FDA Inspection 1276324 - Hiossen, Inc - July 23, 2025

Source: https://www.keypedia.com/records/fda_inspections/hiossen-inc/382bf23b-ca3b-43ac-a6e5-25ece134fadf
Source feed: FDA_Inspections

> FDA Inspection 1276324 for Hiossen, Inc on July 23, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276324
- Company Name: Hiossen, Inc
- Inspection Date: 2025-07-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276324 - 2025-07-23](https://www.keypedia.com/records/fda_inspections/hiossen-inc/bec4a4d3-e023-4a7b-a9c4-25d227ba7bab)

Company: https://www.keypedia.com/companies/hiossen-inc/54e2eabd-a117-4c32-b75d-56956ffcca5c

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