# Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. – FDA Inspection, Aug 26, 2010

Source: https://www.keypedia.com/records/fda_inspections/flextronics-medical-device-manufacturingshenzhen-co-ltd/4c73e953-84e5-4049-a1c9-c60398b0fdce
Source feed: FDA_Inspections

> FDA inspection 683815 of Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd., August 26, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 683815
- Company Name: Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.
- Inspection Date: 2010-08-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 957171 - 2016-02-03
- [FDA Inspection 831935 - 2013-04-17](https://www.keypedia.com/records/fda_inspections/flextronics-medical-device-manufacturingshenzhen-co-ltd/622c4657-8f41-425a-a459-6b0eab31f409)

Company: https://www.keypedia.com/companies/flextronics-medical-device-manufacturingshenzhen-co-ltd/0beaf98b-4187-4bbb-82d0-639a79c69349

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