# Viant Medical – FDA Inspection, Jun 12, 2023

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

> FDA inspection 1210396 of Viant Medical, June 12, 2023. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1044026 - 2018-02-20](https://www.keypedia.com/records/fda_inspections/viant-medical/b14a4740-83cd-4539-bb9b-d386c2c42bc9)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brittani-n-franklin/1d5e9344-1145-42ff-a175-5541b565b15e)

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

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