# FDA Inspection 920344 - Shenzhen Healthway Electronics  Co.Ltd - March 26, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-healthway-electronics-coltd/f3821ad4-35f7-48e6-ad13-faafc7e10728
Source feed: FDA_Inspections

> FDA Inspection 920344 for Shenzhen Healthway Electronics  Co.Ltd on March 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920344
- Company Name: Shenzhen Healthway Electronics  Co.Ltd
- Inspection Date: 2015-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1039328 - 2017-12-07](https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-healthway-electronics-coltd/9156e358-98e2-49e2-a5ca-9c46507ab73e)
- [FDA Inspection 771200 - 2012-03-02](https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-healthway-electronics-coltd/c902a2ba-02a4-4c0a-9137-a6153fa99666)

Company: https://www.globalkeysolutions.net/companies/shenzhen-healthway-electronics-coltd/ff1c2508-3c89-48c3-bdac-5da8ec5318d7

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