# FDA Inspection 1008820 - CORTRONIK GmbH - March 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/cortronik-gmbh/97aad66d-1d63-4156-a399-96f9d2e9e2bf
Source feed: FDA_Inspections

> FDA Inspection 1008820 for CORTRONIK GmbH on March 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008820
- Company Name: CORTRONIK GmbH
- Inspection Date: 2017-03-02
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1086324 - 2019-01-17](https://www.keypedia.com/records/fda_inspections/cortronik-gmbh/4e6e9403-9b19-4d4f-8d8c-af3dc1608d27)
- [FDA Inspection 1008820 - 2017-03-02](https://www.keypedia.com/records/fda_inspections/cortronik-gmbh/d4a47227-51f4-46e3-a449-24821372a6e0)

Company: https://www.keypedia.com/companies/cortronik-gmbh/28408b7f-bf52-471f-af77-533a2e0223f5

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