FDA inspection
Ziosoft USA, Inc.: FDA inspection ending May 15, 2013
FDA inspection 833418 · Voluntary Action Indicated (VAI) · Newark, CA
Key facts
| Inspection ID | 833418 |
|---|---|
| Firm | Ziosoft USA, Inc. |
| FEI number | 3009394491 |
| Address | 39899 Balentine Dr Ste 116 |
| City | Newark |
| State | CA |
| ZIP | 94560 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | May 15, 2013 |
| 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