# Shenzhen Healthway Electronics  Co.Ltd – FDA Inspection, Dec 7, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-healthway-electronics-coltd/9156e358-98e2-49e2-a5ca-9c46507ab73e
Source feed: FDA_Inspections

> FDA inspection 1039328 of Shenzhen Healthway Electronics  Co.Ltd, December 07, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1039328
- Company Name: Shenzhen Healthway Electronics  Co.Ltd
- Inspection Date: 2017-12-07
- 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: 0

## Related Documents

- [FDA Inspection 920344 - 2015-03-26](https://www.keypedia.com/records/fda_inspections/shenzhen-healthway-electronics-coltd/f3821ad4-35f7-48e6-ad13-faafc7e10728)
- FDA Inspection 771200 - 2012-03-02

## Related Officers

- [Sean T. Creighton](https://www.keypedia.com/people/sean-t-creighton/80ffecab-0a2d-4727-a11f-407b697f4503)

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