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FDA Inspection
•Dr. Japan Co., Ltd.•November 9, 2017

Dr. Japan Co., Ltd. – FDA Inspection, Nov 9, 2017

Record Details

This FDA Inspection record concerns Dr. Japan Co., Ltd., with an inspection on November 9, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Dr. Japan Co., Ltd.
Inspection Date
November 9, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Thai T. Duong (Issuing Officer)
View Company Profile

ID · b3f0e794-0863-4ed0-844f-29fe77aadea5

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1034026
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

Other FDA inspections of Dr. Japan Co., Ltd.

1
DateClassificationOfficeProject area
June 28, 2015VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Dr. Japan Co., Ltd.
  • FDA Inspection 933520 - 2015-06-28

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