# Shenzhen Healthway Electronics  Co.Ltd – FDA Inspection, Mar 26, 2015

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

> FDA inspection 920344 of Shenzhen Healthway Electronics  Co.Ltd, March 26, 2015. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1039328 - 2017-12-07](https://www.keypedia.com/records/fda_inspections/shenzhen-healthway-electronics-coltd/9156e358-98e2-49e2-a5ca-9c46507ab73e)
- FDA Inspection 771200 - 2012-03-02

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

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