FDA Inspection 1248233 — Shenzhen Aeon Technology Co., Ltd.
The FDA completed an inspection of Shenzhen Aeon Technology Co., Ltd. on Aug 1, 2024 in Shenzhen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 1, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)