# FDA Inspection 1099573 - Curetis Gmbh - February 14, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/curetis-gmbh/37d71f92-589d-40c1-a2bd-28871958f428
Source feed: FDA_Inspections

> FDA Inspection 1099573 for Curetis Gmbh on February 14, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099573
- Company Name: Curetis Gmbh
- Inspection Date: 2019-02-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1099573 - 2019-02-14](https://www.globalkeysolutions.net/records/fda_inspections/curetis-gmbh/b7af3c06-5df2-43cb-8428-b324f92d9a6d)

Company: https://www.globalkeysolutions.net/companies/curetis-gmbh/93a43d40-b28f-473f-a6e4-af3f9a1f32be

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