# FDA Inspection 1102228 - Mondeal Medical Systems Gmbh - September 19, 2019

Source: https://www.keypedia.com/records/fda_inspections/mondeal-medical-systems-gmbh/d6b2e1a3-87bb-4bdc-8c12-c9e5884704cb
Source feed: FDA_Inspections

> FDA Inspection 1102228 for Mondeal Medical Systems Gmbh on September 19, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102228
- Company Name: Mondeal Medical Systems Gmbh
- Inspection Date: 2019-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1102228 - 2019-09-19](https://www.keypedia.com/records/fda_inspections/mondeal-medical-systems-gmbh/7e050d87-a236-44a7-b581-aca83ba60ed4)
- [FDA Inspection 865973 - 2014-01-24](https://www.keypedia.com/records/fda_inspections/mondeal-medical-systems-gmbh/d846ef93-70d9-4575-95b3-7f8b7c512b72)

Company: https://www.keypedia.com/companies/mondeal-medical-systems-gmbh/3c5d3cef-3c71-40b2-b28a-508d863fd90a

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