FDA inspection
EMG Technology Co., Ltd.: FDA inspection ending Aug 17, 2017
FDA inspection 1024829 · Voluntary Action Indicated (VAI) · Taichung City
Key facts
| Inspection ID | 1024829 |
|---|---|
| Firm | EMG Technology Co., Ltd. |
| FEI number | 3003803075 |
| Address | Xitun District, No. 58 Gongyequ 35th Rd.; Xitun Dist. |
| City | Taichung City |
| Country | Taiwan |
| Fiscal year | 2017 |
| Inspection end date | Aug 17, 2017 |
| 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