FDA Inspection
Mindray DS USA, Inc. dba Mindray North AmericaFDA Inspection 849828 - Mindray DS USA, Inc. dba Mindray North America - September 23, 2013
Record Details
This FDA Inspection record concerns Mindray DS USA, Inc. dba Mindray North America, with an inspection on September 23, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 23, 2013
- Product Type
- Devices
View Company Profile
ID · a54e041d-29c2-4d6e-9b4c-b258ae88bccd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 849828
- 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 |
| March 10, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: 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 910764 - 2015-03-10
- FDA Inspection 795266 - 2012-08-02
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