# FDA Inspection 668336 - Mindray DS USA, Inc. dba Mindray North America - June 10, 2010

Source: https://www.keypedia.com/records/fda_inspections/mindray-ds-usa-inc-dba-mindray-north-america/b61a2a8d-7bf6-4c2b-89b6-78c858d5e6c7
Source feed: FDA_Inspections

> FDA inspection 668336 of Mindray DS USA, Inc. dba Mindray North America, June 10, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations 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: 668336
- Company Name: Mindray DS USA, Inc. dba Mindray North America
- Inspection Date: 2010-06-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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- [FDA Inspection 968103 - 2016-03-31](https://www.keypedia.com/records/fda_inspections/mindray-ds-usa-inc-dba-mindray-north-america/2b9c3d57-be90-4c86-a345-418e4d9f795a)
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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