FDA inspection
Theranos, Inc.: FDA inspection ending Sep 16, 2015
FDA inspection 942922 · Voluntary Action Indicated (VAI) · Newark, CA
Key facts
| Inspection ID | 942922 |
|---|---|
| Firm | Theranos, Inc. |
| FEI number | 3006231732 |
| Address | 7333 Gateway Blvd |
| City | Newark |
| State | CA |
| ZIP | 94560 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Sep 16, 2015 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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