FDA inspection
Jiangyin PureMED Products Co., Ltd.: FDA inspection ending May 23, 2019
FDA inspection 1093743 · Voluntary Action Indicated (VAI) · Jiangyin
Key facts
| Inspection ID | 1093743 |
|---|---|
| Firm | Jiangyin PureMED Products Co., Ltd. |
| FEI number | 3008352384 |
| Address | Huaxi Industrial Park 22, 1 South Huancun Road; Hua Town |
| City | Jiangyin |
| Country | China |
| Fiscal year | 2019 |
| Inspection end date | May 23, 2019 |
| 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