# FDA Inspection 1172424 - ReFlow Medical - June 09, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/reflow-medical/fa771354-70ce-42c3-b39f-c67113f30177/
Source feed: FDA_Inspections

> FDA Inspection 1172424 for ReFlow Medical on June 09, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1172424
- Company Name: ReFlow Medical
- Inspection Date: 2022-06-09
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1172424 - 2022-06-09](https://www.globalkeysolutions.net/api/records/fda_inspections/reflow-medical/70f6cd67-4bb4-44b2-a59b-7e9cef26b09f/)
- [FDA Inspection 1079508 - 2018-11-28](https://www.globalkeysolutions.net/api/records/fda_inspections/reflow-medical/5b5200ea-b014-4c08-8340-6560bdaafb6a/)
- [FDA Inspection 1079508 - 2018-11-28](https://www.globalkeysolutions.net/api/records/fda_inspections/reflow-medical/70c62cd3-63e0-42d1-8895-4bb5ec2678c6/)
- [FDA Inspection 916547 - 2015-02-26](https://www.globalkeysolutions.net/api/records/fda_inspections/reflow-medical/f52ac186-99d8-4e25-a58c-74da3634dab8/)
- [FDA Inspection 916547 - 2015-02-26](https://www.globalkeysolutions.net/api/records/fda_inspections/reflow-medical/23352655-4e05-4a5b-9360-f1cfa0774777/)

Company: https://www.globalkeysolutions.net/companies/reflow-medical/30995a3a-4434-4a34-b32d-44f4fa7c57a9

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7