FDA Inspection 1336308 — Heartbeam
The FDA completed an inspection of Heartbeam on Sep 16, 2026 in Santa Clara, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 16, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Santa Clara, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 23219 | ISO 13485:2016 Clause 8.2.2 | Complaint handling records not maintained |