FDA inspection
NRT X-RAY A/S: FDA inspection ending Feb 6, 2026
FDA inspection 1301478 · Hasselager
Key facts
| Inspection ID | 1301478 |
|---|---|
| Firm | NRT X-RAY A/S |
| FEI number | 1000188474 |
| Address | Birkegaardsvej 16 |
| City | Hasselager |
| Fiscal year | 2026 |
| Inspection end date | Feb 6, 2026 |
| Project area | Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Compliance: Medical Devices|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority|Postmarket Assurance: Medical Devices|Radiation Control and Health Safety Act (RCHSA) Authority |
| 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