FDA inspection
Daheng New Epoch Technology, Inc.: FDA inspection ending Jul 14, 2017
FDA inspection 1019785 · Voluntary Action Indicated (VAI) · Beijing
Key facts
| Inspection ID | 1019785 |
|---|---|
| Firm | Daheng New Epoch Technology, Inc. |
| FEI number | 3008705657 |
| Address | # A9, Shangdi Xinxilu; Haidian District |
| City | Beijing |
| Country | China |
| Fiscal year | 2017 |
| Inspection end date | Jul 14, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| Product type | Devices |
At a glance
- 1–9 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