FDA Inspection
Typhoon Water Wares LimitedTyphoon Water Wares Limited – FDA Inspection, Jul 19, 2017
Record Details
This FDA Inspection record concerns Typhoon Water Wares Limited, with an inspection on July 19, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b55e4c92-de78-499e-af15-ce5f33881b8e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019169
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Typhoon Water Wares Limited
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 4, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 28, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 1, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Typhoon Water Wares Limited
- FDA Inspection 883865 - 2014-06-04
- FDA Inspection 837902 - 2013-06-28
- FDA Inspection 790636 - 2012-08-01
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