FDA inspection
Jiangsu Likang Medical Products Co., LTD: FDA inspection ending Dec 16, 2004
FDA inspection 365324 · Voluntary Action Indicated (VAI) · Suzhou
Key facts
| Inspection ID | 365324 |
|---|---|
| Firm | Jiangsu Likang Medical Products Co., LTD |
| FEI number | 3001751372 |
| Address | 2191 Beishe Street, Fenhu Zhen Wujiang |
| City | Suzhou |
| Fiscal year | 2005 |
| Inspection end date | Dec 16, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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