FDA inspection
Primed Liyang Medical Products Mfg. Co., Ltd.: FDA inspection ending Apr 24, 2014
FDA inspection 880862 · Voluntary Action Indicated (VAI) · Changzhou
Key facts
| Inspection ID | 880862 |
|---|---|
| Firm | Primed Liyang Medical Products Mfg. Co., Ltd. |
| FEI number | 3005599545 |
| Address | Daitoucun, Daitouzhen Liyang |
| City | Changzhou |
| Country | China |
| Fiscal year | 2014 |
| Inspection end date | Apr 24, 2014 |
| 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