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FDA Inspection
•Regenesis Biomedical Inc•May 16, 2017

Regenesis Biomedical Inc – FDA Inspection, May 16, 2017

Record Details

This FDA Inspection record concerns Regenesis Biomedical Inc, with an inspection on May 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Regenesis Biomedical Inc
Inspection Date
May 16, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Charles L. Larson (Company Rep)
View Company Profile

ID · 30fb3abc-44d9-4324-a32c-ea49ba85e833

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1024124
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Regenesis Biomedical Inc

3
DateClassificationOfficeProject area
June 11, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
November 9, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
July 20, 2009NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Regenesis Biomedical Inc
  • FDA Inspection 838831 - 2013-06-11
  • FDA Inspection 752842 - 2011-11-09
  • FDA Inspection 599980 - 2009-07-20

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