# FDA Inspection 1294388 - Heartvista, Inc. dba Vista.ai - October 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/heartvista-inc-dba-vistaai/8188ed8e-d19b-41a6-ad05-df6c7a8475df
Source feed: FDA_Inspections

> FDA Inspection 1294388 for Heartvista, Inc. dba Vista.ai on October 30, 2025. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1294388
- Company Name: Heartvista, Inc. dba Vista.ai
- Inspection Date: 2025-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1294388 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/heartvista-inc-dba-vistaai/469280e8-c993-438a-852c-81a482503f26)
- [FDA Inspection 1294388 - 2025-10-30](https://www.keypedia.com/records/fda_inspections/heartvista-inc-dba-vistaai/73b11440-1575-4862-b391-3374d300fbbc)

Company: https://www.keypedia.com/companies/heartvista-inc-dba-vistaai/9dad3b07-8754-4ae6-b6a1-83289bdc19f2

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