FDA inspection
Shenzhen Aeon Technology Co., Ltd.: FDA inspection ending Aug 1, 2024
FDA inspection 1248233 · Voluntary Action Indicated (VAI) · Shenzhen
Key facts
| Inspection ID | 1248233 |
|---|---|
| Firm | Shenzhen Aeon Technology Co., Ltd. |
| FEI number | 3008830133 |
| Address | Building A A301, No. 5003 Bao'An Avenue; Baoan |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2024 |
| Inspection end date | Aug 1, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data