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FDA Inspection
•Cheen Houng Enterprise Co., Ltd.•November 22, 2018

Cheen Houng Enterprise Co., Ltd. – FDA Inspection, Nov 22, 2018

Record Details

This FDA Inspection record concerns Cheen Houng Enterprise Co., Ltd., with an inspection on November 22, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cheen Houng Enterprise Co., Ltd.
Inspection Date
November 22, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Thai T. Duong (Issuing Officer)
View Company Profile

ID · 7874766b-376c-40aa-8777-151fe52ad17c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1074500
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Cheen Houng Enterprise Co., Ltd.

4
DateClassificationOfficeProject area
April 10, 2024NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 21, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
August 8, 2013OAICenter for Devices and Radiological HealthCompliance: Devices
December 17, 2009VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Cheen Houng Enterprise Co., Ltd.
  • FDA Inspection 1237498 - 2024-04-10
  • FDA Inspection 969359 - 2016-04-21
  • FDA Inspection 844111 - 2013-08-08
  • FDA Inspection 638732 - 2009-12-17

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