# ReFlow Medical – FDA Inspection, Feb 26, 2015

Source: https://www.keypedia.com/records/fda_inspections/reflow-medical/f52ac186-99d8-4e25-a58c-74da3634dab8
Source feed: FDA_Inspections

> FDA inspection 916547 of ReFlow Medical, February 26, 2015. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 916547
- Company Name: ReFlow Medical
- Inspection Date: 2015-02-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1172424 - 2022-06-09](https://www.keypedia.com/records/fda_inspections/reflow-medical/fa771354-70ce-42c3-b39f-c67113f30177)
- FDA Inspection 1079508 - 2018-11-28

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

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