FDA inspection
DIO USA: FDA inspection ending May 12, 2010
FDA inspection 661058 · Voluntary Action Indicated (VAI) · Los Angeles, CA
Key facts
| Inspection ID | 661058 |
|---|---|
| Firm | DIO USA |
| FEI number | 3006400105 |
| Address | 3540 Wilshire Blvd Ste 1104 |
| City | Los Angeles |
| State | CA |
| ZIP | 90010 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | May 12, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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