FDA Inspection
Mindray DS USA, Inc. dba Mindray North AmericaFDA Inspection 1062457 - Mindray DS USA, Inc. dba Mindray North America - April 20, 2018
Record Details
This FDA Inspection record concerns Mindray DS USA, Inc. dba Mindray North America, with an inspection on April 20, 2018, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- April 20, 2018
- Product Type
- Devices
View Company Profile
ID · 2e9a32b1-1596-4fa7-9ad8-988b96562adc
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1062457
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Mindray DS USA, Inc. dba Mindray North America
6| Date | Classification | Office | Project area |
|---|---|---|---|
| February 22, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 31, 2016 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 10, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 23, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 2, 2012 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Mindray DS USA, Inc. dba Mindray North America
- FDA Inspection 1251239 - 2024-02-22
- FDA Inspection 968103 - 2016-03-31
- FDA Inspection 910764 - 2015-03-10
- FDA Inspection 849828 - 2013-09-23
- FDA Inspection 795266 - 2012-08-02
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