FDA inspection
Mindray DS USA, Inc.: FDA inspection ending Sep 23, 2013
FDA inspection 849828 · Voluntary Action Indicated (VAI) · Mahwah, NJ
Key facts
| Inspection ID | 849828 |
|---|---|
| Firm | Mindray DS USA, Inc. |
| FEI number | 2221819 |
| Address | 800 Macarthur Blvd |
| City | Mahwah |
| State | NJ |
| ZIP | 07430 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Sep 23, 2013 |
| 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
- 10–99 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