# FDA Inspection 1094151 - Desyncra Operating Gmbh - May 16, 2019

Source: https://www.keypedia.com/records/fda_inspections/desyncra-operating-gmbh/6b5bb29a-57e2-45e2-b004-ea921cf64aa8
Source feed: FDA_Inspections

> FDA Inspection 1094151 for Desyncra Operating Gmbh on May 16, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094151
- Company Name: Desyncra Operating Gmbh
- Inspection Date: 2019-05-16
- 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 1094151 - 2019-05-16](https://www.keypedia.com/records/fda_inspections/desyncra-operating-gmbh/71d625c9-e284-4269-8638-61448b222589)

Company: https://www.keypedia.com/companies/desyncra-operating-gmbh/ca069091-d1f2-49f2-96e9-e99f421143d2

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