FDA Inspection 1294388 — Heartvista, Inc.
The FDA completed an inspection of Heartvista, Inc. on October 30, 2025 in Palo Alto, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- October 30, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Palo Alto, CA (United States)