# FDA Inspection 1057371 - Nouvag Ag - June 21, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/nouvag-ag/64d65260-da5f-456c-9397-f1c846d3a69c
Source feed: FDA_Inspections

> FDA Inspection 1057371 for Nouvag Ag on June 21, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057371
- Company Name: Nouvag Ag
- Inspection Date: 2018-06-21
- 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 1057371 - 2018-06-21](https://www.globalkeysolutions.net/records/fda_inspections/nouvag-ag/60fbb67e-e114-4393-9264-99605dc0db63)
- [FDA Inspection 970047 - 2016-05-12](https://www.globalkeysolutions.net/records/fda_inspections/nouvag-ag/6f8759d2-31e7-4e14-be35-e2c08bac5f7f)
- [FDA Inspection 970047 - 2016-05-12](https://www.globalkeysolutions.net/records/fda_inspections/nouvag-ag/4e6813e9-d7ab-4fb6-ae9a-ed273f58f011)

Company: https://www.globalkeysolutions.net/companies/nouvag-ag/0ba4ed5b-69a4-4332-9003-98c2820193cf

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