# FDA Inspection 1210396 - Viant Medical - June 12, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/viant-medical/fe6e7c4f-2703-4d99-a43c-4abc9002f51f
Source feed: FDA_Inspections

> FDA Inspection 1210396 for Viant Medical on June 12, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1210396
- Company Name: Viant Medical
- Inspection Date: 2023-06-12
- 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 1210396 - 2023-06-12](https://www.globalkeysolutions.net/records/fda_inspections/viant-medical/6170a9be-bfe1-4a7d-8fd5-fb39e7a1b1c3)
- [FDA Inspection 1044026 - 2018-02-20](https://www.globalkeysolutions.net/records/fda_inspections/viant-medical/13796e5d-dfa6-4db3-8e48-4abe77da5c1d)
- [FDA Inspection 1044026 - 2018-02-20](https://www.globalkeysolutions.net/records/fda_inspections/viant-medical/b14a4740-83cd-4539-bb9b-d386c2c42bc9)

Company: https://www.globalkeysolutions.net/companies/viant-medical/58a2f771-62bc-4b74-8e88-e321de8d2e16

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