FDA inspection
Suzhou Kangli Orthopaedics Instrument Co., Ltd.: FDA inspection ending Jun 14, 2018
FDA inspection 1069150 · No Action Indicated (NAI) · Suzhou
Key facts
| Inspection ID | 1069150 |
|---|---|
| Firm | Suzhou Kangli Orthopaedics Instrument Co., Ltd. |
| FEI number | 3008749819 |
| Address | Hedong Road, Zhangjiagang |
| City | Suzhou |
| Country | China |
| Fiscal year | 2018 |
| Inspection end date | Jun 14, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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