FDA Inspection
Mindray DS USA, Inc. dba Mindray North AmericaFDA Inspection 910764 - Mindray DS USA, Inc. dba Mindray North America - March 10, 2015
Record Details
This FDA Inspection record concerns Mindray DS USA, Inc. dba Mindray North America, with an inspection on March 10, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 10, 2015
- Product Type
- Devices
View Company Profile
ID · 073d6b3a-9b52-4c4d-be01-fdf13d931e4c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 910764
- 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 |
| April 20, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 31, 2016 | OAI | 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 1062457 - 2018-04-20
- FDA Inspection 968103 - 2016-03-31
- FDA Inspection 849828 - 2013-09-23
- FDA Inspection 795266 - 2012-08-02
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