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FDA Inspection
•Taicang Kanghui Technology Development Company, Ltd.•September 21, 2017

Taicang Kanghui Technology Development Company, Ltd. – FDA Inspection, Sep 21, 2017

Record Details

This FDA Inspection record concerns Taicang Kanghui Technology Development Company, Ltd., with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Taicang Kanghui Technology Development Company, Ltd.
Inspection Date
September 21, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Thai T. Duong (Issuing Officer)
View Company Profile

ID · 583ad9ea-4d49-4510-be1e-9e5a04d41ca6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1029014
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Taicang Kanghui Technology Development Company, Ltd.

1
DateClassificationOfficeProject area
May 21, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Taicang Kanghui Technology Development Company, Ltd.
  • FDA Inspection 884269 - 2014-05-21

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