FDA inspection
Allmed Medical Products Co., Ltd. (Zhijiang Factory): FDA inspection ending Feb 25, 2016
FDA inspection 964578 · No Action Indicated (NAI) · Yichang
Key facts
| Inspection ID | 964578 |
|---|---|
| Firm | Allmed Medical Products Co., Ltd. (Zhijiang Factory) |
| FEI number | 3004950768 |
| Address | 180 Gongyuanlu, Zhijiang |
| City | Yichang |
| Country | China |
| Fiscal year | 2016 |
| Inspection end date | Feb 25, 2016 |
| 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