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FDA Inspection
•OriGen Biomedical, Inc.•January 8, 2020

OriGen Biomedical, Inc. – FDA Inspection, Jan 8, 2020

Record Details

This FDA Inspection record concerns OriGen Biomedical, Inc., with an inspection on January 8, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company
OriGen Biomedical, Inc.
Inspection Date
January 8, 2020
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 58c4e34f-5444-408a-9a2a-b9241ea96457

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1115852
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of OriGen Biomedical, Inc.

2
DateClassificationOfficeProject area
July 5, 2018OAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 26, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for OriGen Biomedical, Inc.
  • FDA Inspection 1059095 - 2018-07-05
  • FDA Inspection 828408 - 2013-04-26

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