# FDA Inspection 916547 - ReFlow Medical - February 26, 2015

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

> FDA Inspection 916547 for ReFlow Medical on February 26, 2015. Classification: No Action Indicated (NAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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