FDA inspection
Shenzhen Kaiyan Medical Equipment Limited: FDA inspection ending Oct 25, 2017
FDA inspection 1032564 · No Action Indicated (NAI) · Shenzhen
Key facts
| Inspection ID | 1032564 |
|---|---|
| Firm | Shenzhen Kaiyan Medical Equipment Limited |
| FEI number | 3011644607 |
| Address | 40A Fuxin Road Fuyong Subdistrict, Baoan District |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2018 |
| Inspection end date | Oct 25, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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