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FDA Inspection
•ReFlow Medical•June 9, 2022

ReFlow Medical – FDA Inspection, Jun 9, 2022

Record Details

This FDA Inspection record concerns ReFlow Medical, with an inspection on June 9, 2022, issued by the Center for Devices and Radiological Health, covering devices.

Company
ReFlow Medical
Inspection Date
June 9, 2022
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · fa771354-70ce-42c3-b39f-c67113f30177

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1172424
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of ReFlow Medical

2
DateClassificationOfficeProject area
November 28, 2018NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
February 26, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for ReFlow Medical
  • FDA Inspection 1079508 - 2018-11-28
  • FDA Inspection 916547 - 2015-02-26

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