# FDA Inspection 1248233 - Shenzhen Aeon Technology Co., Ltd. - August 01, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-aeon-technology-co-ltd/daf7bd08-a31e-442b-ae7a-90c6f40a8b34
Source feed: FDA_Inspections

> FDA Inspection 1248233 for Shenzhen Aeon Technology Co., Ltd. on August 01, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1248233
- Company Name: Shenzhen Aeon Technology Co., Ltd.
- Inspection Date: 2024-08-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1248233 - 2024-08-01](https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-aeon-technology-co-ltd/025a7732-d4c0-40c7-b371-33202bee345b)

Company: https://www.globalkeysolutions.net/companies/shenzhen-aeon-technology-co-ltd/0ee0e010-ae22-48d6-8ed1-1d337e11d233

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