# FDA Inspection 968103 - Mindray DS USA, Inc. dba Mindray North America - March 31, 2016

Source: https://www.keypedia.com/records/fda_inspections/mindray-ds-usa-inc-dba-mindray-north-america/1cb230b6-62b6-401a-bf97-be87aa626548
Source feed: FDA_Inspections

> FDA inspection 968103 of Mindray DS USA, Inc. dba Mindray North America, March 31, 2016. Classification: Official Action Indicated (OAI). 1 citation under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 968103
- Company Name: Mindray DS USA, Inc. dba Mindray North America
- Inspection Date: 2016-03-31
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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- [FDA Inspection 910764 - 2015-03-10](https://www.keypedia.com/records/fda_inspections/mindray-ds-usa-inc-dba-mindray-north-america/53d4dfa6-a4a8-4752-b976-25dc3bb87dae)
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Company: https://www.keypedia.com/companies/mindray-ds-usa-inc-dba-mindray-north-america/036bf79f-c69c-44bb-bdd6-65381d7eb1c4

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
