FDA inspection
Diatron MI Plc: FDA inspection ending Nov 20, 2025
FDA inspection 1301970 · No Action Indicated (NAI) · Budapest
Key facts
| Inspection ID | 1301970 |
|---|---|
| Firm | Diatron MI Plc |
| FEI number | 3009297077 |
| Address | Tablas Utca 39 |
| City | Budapest |
| Country | Hungary |
| Fiscal year | 2026 |
| Inspection end date | Nov 20, 2025 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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