FDA inspection
Mindray DS USA, Inc.: FDA inspection ending Apr 20, 2018
FDA inspection 1062457 · No Action Indicated (NAI) · Mahwah, NJ
Key facts
| Inspection ID | 1062457 |
|---|---|
| Firm | Mindray DS USA, Inc. |
| FEI number | 2221819 |
| Address | 800 Macarthur Blvd |
| City | Mahwah |
| State | NJ |
| ZIP | 07430 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Apr 20, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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