FDA inspection
SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD.: FDA inspection ending Mar 27, 2014
FDA inspection 875112 · Voluntary Action Indicated (VAI) · Shanghai
Key facts
| Inspection ID | 875112 |
|---|---|
| Firm | SHANGHAI APOLO MEDICAL TECHNOLOGY CO., LTD. |
| FEI number | 3007120647 |
| Address | Room 301-310, Building 11, No. 388, Yindu Road, Xuhui District |
| City | Shanghai |
| Country | China |
| Fiscal year | 2014 |
| Inspection end date | Mar 27, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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