# FDA Inspection 1272862 - ORIGIN MEDICAL DEVICES HUNGARY KFT - May 08, 2025

Source: https://www.keypedia.com/records/fda_inspections/origin-medical-devices-hungary-kft/6f9a4945-fd2a-4f5e-b6f4-ac0a1ded17d1
Source feed: FDA_Inspections

> FDA Inspection 1272862 for ORIGIN MEDICAL DEVICES HUNGARY KFT on May 08, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1272862
- Company Name: ORIGIN MEDICAL DEVICES HUNGARY KFT
- Inspection Date: 2025-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1272862 - 2025-05-08](https://www.keypedia.com/records/fda_inspections/origin-medical-devices-hungary-kft/034d2a2b-ab0e-423e-86b5-b97179fffa77)
- [FDA Inspection 1272862 - 2025-05-08](https://www.keypedia.com/records/fda_inspections/origin-medical-devices-hungary-kft/c4a5d6a5-ac65-4108-8400-bdb8c59bbd67)

Company: https://www.keypedia.com/companies/origin-medical-devices-hungary-kft/3c6f6d9f-87d0-40d8-99df-1eaf1a5f5a9b

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7