# FDA Inspection 1014030 - Curasan AG, Frankfurt Facility - May 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/curasan-ag-frankfurt-facility/6e833014-fe85-4e91-afc3-79305276d3d6
Source feed: FDA_Inspections

> FDA Inspection 1014030 for Curasan AG, Frankfurt Facility on May 11, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014030
- Company Name: Curasan AG, Frankfurt Facility
- Inspection Date: 2017-05-11
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1014030 - 2017-05-11](https://www.keypedia.com/records/fda_inspections/curasan-ag-frankfurt-facility/167343f6-cd51-48e2-b015-7c3859951b53)

Company: https://www.keypedia.com/companies/curasan-ag-frankfurt-facility/ce15097d-f383-4641-9bac-ed4d724b6d32

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