FDA inspection
Terumo Medical Products (Hangzhou) Co., Ltd.: FDA inspection ending Mar 22, 2018
FDA inspection 1077793 · Voluntary Action Indicated (VAI) · Hangzhou
Key facts
| Inspection ID | 1077793 |
|---|---|
| Firm | Terumo Medical Products (Hangzhou) Co., Ltd. |
| FEI number | 3004102031 |
| Address | 5 M4-9 Economic & Technological, Development Zone |
| City | Hangzhou |
| Fiscal year | 2018 |
| Inspection end date | Mar 22, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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