FDA inspection
Cardiva Medical, Inc.: FDA inspection ending May 10, 2017
FDA inspection 1014545 · Voluntary Action Indicated (VAI) · Santa Clara, CA
Key facts
| Inspection ID | 1014545 |
|---|---|
| Firm | Cardiva Medical, Inc. |
| FEI number | 3015145497 |
| Address | 2900 Lakeside Dr Ste 160 |
| City | Santa Clara |
| State | CA |
| ZIP | 95054 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | May 10, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 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