FDA inspection
Ryder Electronics (Shenzhen) Ltd: FDA inspection ending Jul 11, 2025
FDA inspection 1276637 · No Action Indicated (NAI) · Shenzhen
Key facts
| Inspection ID | 1276637 |
|---|---|
| Firm | Ryder Electronics (Shenzhen) Ltd |
| FEI number | 3011235999 |
| Address | 139 Da Bao Road, Baoan District |
| City | Shenzhen |
| Fiscal year | 2025 |
| Inspection end date | Jul 11, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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