FDA Inspection
Mindray DS USA, Inc. dba Mindray North AmericaFDA Inspection 1251239 - Mindray DS USA, Inc. dba Mindray North America - February 22, 2024
Record Details
This FDA Inspection record concerns Mindray DS USA, Inc. dba Mindray North America, with an inspection on February 22, 2024, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 22, 2024
- Product Type
- Devices
- Person
- Melissa A. Zuppe
View Company Profile
ID · 46dc03b2-679a-47fe-9d85-35252653fecb
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1251239
- 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 |
|---|---|---|---|
| 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 |
| 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 1062457 - 2018-04-20
- 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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