FDA inspection
Terumo Medical Products (Hangzhou) Co., Ltd.: FDA inspection ending Oct 29, 2015
FDA inspection 948623 · No Action Indicated (NAI) · Hangzhou
Key facts
| Inspection ID | 948623 |
|---|---|
| Firm | Terumo Medical Products (Hangzhou) Co., Ltd. |
| FEI number | 3004102031 |
| Address | 5 M4-9 Economic & Technological, Development Zone |
| City | Hangzhou |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Oct 29, 2015 |
| 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