FDA inspection
Guangdong Baihe Medical Technology Co., Ltd: FDA inspection ending Aug 24, 2017
FDA inspection 1027009 · Voluntary Action Indicated (VAI) · Foshan
Key facts
| Inspection ID | 1027009 |
|---|---|
| Firm | Guangdong Baihe Medical Technology Co., Ltd |
| FEI number | 3006621386 |
| Address | Building 2, Building3-6f Building F 3-4, No. 89 Taoyuan East Road |
| City | Foshan |
| Country | China |
| Fiscal year | 2017 |
| Inspection end date | Aug 24, 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