# FDA Inspection 1283806 - Viant Medical Company - September 26, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/viant-medical-company/dd143a25-13b4-4eb2-9422-a03a453957cc
Source feed: FDA_Inspections

> FDA Inspection 1283806 for Viant Medical Company on September 26, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283806
- Company Name: Viant Medical Company
- Inspection Date: 2025-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1283806 - 2025-09-26](https://www.globalkeysolutions.net/records/fda_inspections/viant-medical-company/ec7baac5-0aa3-422c-a0a6-9fc7d26591e6)
- [FDA Inspection 939625 - 2015-08-26](https://www.globalkeysolutions.net/records/fda_inspections/viant-medical-company/c228b02b-c501-4508-9952-55eb84d527e5)

Company: https://www.globalkeysolutions.net/companies/viant-medical-company/fcbf7eff-1e92-4ff4-a311-fa64e4262aed

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