# FDA Inspection 683815 - Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. - August 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 for Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. on August 26, 2010. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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