FDA inspection
SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD.: FDA inspection ending Nov 29, 2018
FDA inspection 1088144 · No Action Indicated (NAI) · Shenzhen
Key facts
| Inspection ID | 1088144 |
|---|---|
| Firm | SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD. |
| FEI number | 3006769302 |
| Address | Of Building A F 2 |
| City | Shenzhen |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | Nov 29, 2018 |
| 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