FDA inspection
Shandong Lianfa Medical Plastic Products Co., Ltd: FDA inspection ending Jul 24, 2025
FDA inspection 1278970 · Voluntary Action Indicated (VAI) · Jinan
Key facts
| Inspection ID | 1278970 |
|---|---|
| Firm | Shandong Lianfa Medical Plastic Products Co., Ltd |
| FEI number | 3008801456 |
| Address | 1 Sanjian Road, Shuangshan, Zhangqiu |
| City | Jinan |
| Country | China |
| Fiscal year | 2025 |
| Inspection end date | Jul 24, 2025 |
| 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