# FDA Inspection 957171 - Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. - February 03, 2016

Source: https://www.keypedia.com/records/fda_inspections/flextronics-medical-device-manufacturingshenzhen-co-ltd/33d21e99-7c0b-4ca5-a4ce-493cbfd5478e
Source feed: FDA_Inspections

> FDA Inspection 957171 for Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd. on February 03, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 957171
- Company Name: Flextronics Medical Device Manufacturing(Shenzhen) Co., Ltd.
- Inspection Date: 2016-02-03
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 831935 - 2013-04-17](https://www.keypedia.com/records/fda_inspections/flextronics-medical-device-manufacturingshenzhen-co-ltd/622c4657-8f41-425a-a459-6b0eab31f409)
- [FDA Inspection 683815 - 2010-08-26](https://www.keypedia.com/records/fda_inspections/flextronics-medical-device-manufacturingshenzhen-co-ltd/4c73e953-84e5-4049-a1c9-c60398b0fdce)

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