FDA inspection
Kunshan Jiehong Nonwoven Product Co., Ltd.: FDA inspection ending Jan 23, 2014
FDA inspection 868178 · Voluntary Action Indicated (VAI) · Suzhou
Key facts
| Inspection ID | 868178 |
|---|---|
| Firm | Kunshan Jiehong Nonwoven Product Co., Ltd. |
| FEI number | 3006437555 |
| Address | No. 895 Xinle Road, Dianshanhuzhen Kunshan |
| City | Suzhou |
| Country | China |
| Fiscal year | 2014 |
| Inspection end date | Jan 23, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 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