FDA inspection
YANGZHONG MEDI TECH CO., LTD: FDA inspection ending May 12, 2016
FDA inspection 973310 · No Action Indicated (NAI) · Yangzhong City
Key facts
| Inspection ID | 973310 |
|---|---|
| Firm | YANGZHONG MEDI TECH CO., LTD |
| FEI number | 3005925370 |
| Address | No. 1088 Hongsheng East Zone, Xinba Science and Tech Park |
| City | Yangzhong City |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | May 12, 2016 |
| 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