FDA inspection
Anhui JBH Medical Apparatus Co. Ltd.: FDA inspection ending Sep 11, 2025
FDA inspection 1281378 · Voluntary Action Indicated (VAI) · Chuzhou
Key facts
| Inspection ID | 1281378 |
|---|---|
| Firm | Anhui JBH Medical Apparatus Co. Ltd. |
| FEI number | 3016969129 |
| Address | No. 116 Qicang Road, Industrial Distric Mingguang |
| City | Chuzhou |
| Country | China |
| Fiscal year | 2025 |
| Inspection end date | Sep 11, 2025 |
| 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