FDA inspection
Alivecor, Inc.: FDA inspection ending Oct 5, 2018
FDA inspection 1121934 · Voluntary Action Indicated (VAI) · Mountain View, CA
Key facts
| Inspection ID | 1121934 |
|---|---|
| Firm | Alivecor, Inc. |
| FEI number | 3009715978 |
| Address | 444 Castro St Ste 600 |
| City | Mountain View |
| State | CA |
| ZIP | 94041-2058 |
| Fiscal year | 2019 |
| Inspection end date | Oct 5, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data