FDA inspection
Suzhou Jingle Polymer Medical Apparatus Co., Ltd.: FDA inspection ending Jan 19, 2017
FDA inspection 1013104 · Voluntary Action Indicated (VAI) · Suzhou
Key facts
| Inspection ID | 1013104 |
|---|---|
| Firm | Suzhou Jingle Polymer Medical Apparatus Co., Ltd. |
| FEI number | 3006536657 |
| Address | No. 215 Lian Gangcun, Huqiu Gaoxin |
| City | Suzhou |
| Country | China |
| Fiscal year | 2017 |
| Inspection end date | Jan 19, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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