# NRT X-RAY A/S, Hasselager, Denmark – FDA Inspections

Source: https://www.keypedia.com/companies/nrt-x-ray-as/9dc2935b-a2f9-499d-bda1-66ebc0af0b4a

> Inspection records and compliance data for NRT X-RAY A/S in Hasselager. 4 FDA inspections on record, 2 Form 483s, last inspected February 06, 2026.

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## Details

- Name: NRT X-RAY A/S
- FEI Number: 1000188474
- Address Line 1: Birkegardsvej 16
- City: Hasselager
- Country Name: Denmark
- Address: Birkegardsvej 16, Hasselager, Denmark
- Country: Denmark

## Related Documents

- FDA Inspection 1301478 - NRT X-RAY A/S - 2026-02-06 — source: FDA, date: February 6, 2026
- FDA Inspection 1301478 - NRT X-RAY A/S - 2026-02-06 — source: FDA, date: February 6, 2026
- [FDA Inspection 1301478 - NRT X-RAY A/S - 2026-02-06](https://www.keypedia.com/records/fda_inspections/nrt-x-ray-as/58f1aaa7-1f3e-4f9d-b64d-95d7003b90cc) — source: FDA, date: February 6, 2026
- FDA Inspection 1200620 - NRT X-RAY A/S - 2023-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2023
- [FDA Inspection 1200620 - NRT X-RAY A/S - 2023-03-24](https://www.keypedia.com/records/fda_inspections/nrt-x-ray-as/b800bd85-ed8b-4579-b35b-4b72daba6adf) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2023
- FDA Inspection 1200620 - NRT X-RAY A/S - 2023-03-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 24, 2023
- FDA Inspection 938460 - NRT X-RAY A/S - 2015-07-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2015
- [FDA Inspection 938460 - NRT X-RAY A/S - 2015-07-31](https://www.keypedia.com/records/fda_inspections/nrt-x-ray-as/307f53c6-c840-4950-a20c-e4a64e0da74d) — classification: No Action Indicated (NAI), source: FDA, date: July 31, 2015
- FDA Inspection 938460 - NRT X-RAY A/S - 2015-07-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2015
- FDA Inspection 643990 - NRT X-RAY A/S - 2010-01-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2010

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