FDA inspection
TIANJIN RILIFINE MEDICAL DEVICE CO LTD: FDA inspection ending Jul 31, 2025
FDA inspection 1279097 · Voluntary Action Indicated (VAI) · Tianjin
Key facts
| Inspection ID | 1279097 |
|---|---|
| Firm | TIANJIN RILIFINE MEDICAL DEVICE CO LTD |
| FEI number | 3021314645 |
| Address | No 32 Jingguan Road, Yixingbu, Beichen District |
| City | Tianjin |
| Country | China |
| Fiscal year | 2025 |
| Inspection end date | Jul 31, 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