# FDA Inspection 1047795 - Celitron Medical Technologies Kft - December 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/celitron-medical-technologies-kft/a9f0330e-e80a-49f9-8981-532655e728d6
Source feed: FDA_Inspections

> FDA Inspection 1047795 for Celitron Medical Technologies Kft on December 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047795
- Company Name: Celitron Medical Technologies Kft
- Inspection Date: 2017-12-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 905857 - 2014-11-20](https://www.keypedia.com/records/fda_inspections/celitron-medical-technologies-kft/7931d03c-5abd-4f79-a173-38f70e8c5c8c)

Company: https://www.keypedia.com/companies/celitron-medical-technologies-kft/93164e40-7572-4e78-aa57-35435cc12891

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