FDA inspection
BEIJING HONKON TECHNOLOGIES CO., LTD.: FDA inspection ending Sep 1, 2016
FDA inspection 988018 · Voluntary Action Indicated (VAI) · Beijing
Key facts
| Inspection ID | 988018 |
|---|---|
| Firm | BEIJING HONKON TECHNOLOGIES CO., LTD. |
| FEI number | 3009488834 |
| Address | Building 72 , NO. 16 Huanke Middle Road; Tongzhou |
| City | Beijing |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Sep 1, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| 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