FDA inspection
Guangzhou Improve Medical Instruments Co., Ltd.: FDA inspection ending Jan 17, 2015
FDA inspection 912507 · Voluntary Action Indicated (VAI) · Guangzhou
Key facts
| Inspection ID | 912507 |
|---|---|
| Firm | Guangzhou Improve Medical Instruments Co., Ltd. |
| FEI number | 3008449424 |
| Address | NO. 102 Kaiyuan Avenue, Science City |
| City | Guangzhou |
| Country | China |
| Fiscal year | 2015 |
| Inspection end date | Jan 17, 2015 |
| 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