FDA Inspection
Shenzhen Healthway Electronics Co.LtdShenzhen Healthway Electronics Co.Ltd – FDA Inspection, Dec 7, 2017
Record Details
This FDA Inspection record concerns Shenzhen Healthway Electronics Co.Ltd, with an inspection on December 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 9156e358-98e2-49e2-a5ca-9c46507ab73e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1039328
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Shenzhen Healthway Electronics Co.Ltd
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 2, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Shenzhen Healthway Electronics Co.Ltd
- FDA Inspection 920344 - 2015-03-26
- FDA Inspection 771200 - 2012-03-02
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