# FDA Inspection 1099585 - Curetis GmbH - February 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/curetis-gmbh/bc39d857-a588-46f2-bc67-a267ee0534aa
Source feed: FDA_Inspections

> FDA Inspection 1099585 for Curetis GmbH on February 14, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1099585
- Company Name: Curetis GmbH
- Inspection Date: 2019-02-14
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/curetis-gmbh/c7ebba3e-50eb-47f0-aada-edfad64f7c27

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