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FDA Inspection
•SETO FACTORY OF ASAHI INTECC CO., LTD.•April 30, 2015

SETO FACTORY OF ASAHI INTECC CO., LTD. – FDA Inspection, Apr 30, 2015

Record Details

This FDA Inspection record concerns SETO FACTORY OF ASAHI INTECC CO., LTD., with an inspection on April 30, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
SETO FACTORY OF ASAHI INTECC CO., LTD.
Inspection Date
April 30, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · a4c5d7e0-35a0-4e96-8727-c9220938ab73

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
928339
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of SETO FACTORY OF ASAHI INTECC CO., LTD.

2
DateClassificationOfficeProject area
September 14, 2018Not classifiedOffice of Inspections and Investigations
March 14, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for SETO FACTORY OF ASAHI INTECC CO., LTD.
  • FDA Inspection 1123989 - 2018-09-14
  • FDA Inspection 771558 - 2012-03-14

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