FDA inspection
Tianjin MasterVision Technology Co., Ltd.: FDA inspection ending Aug 31, 2023
FDA inspection 1218181 · Voluntary Action Indicated (VAI) · Tianjin
Key facts
| Inspection ID | 1218181 |
|---|---|
| Firm | Tianjin MasterVision Technology Co., Ltd. |
| FEI number | 3027022707 |
| Address | Building. No. 1st Floor, 15 Heyuan Rd.; Chagugangzhen Wuqing |
| City | Tianjin |
| Fiscal year | 2023 |
| Inspection end date | Aug 31, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Medical 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