# ReFlow Medical – FDA Inspection, Sep 21, 2026

Source: https://www.keypedia.com/records/fda_inspections/reflow-medical/e355cbf9-1a7d-4f99-9bb9-bb03763b9c28
Source feed: FDA_Inspections

> FDA inspection 1336746 of ReFlow Medical, September 21, 2026. Classification: Voluntary Action Indicated (VAI). 2 citations. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1336746
- Company Name: ReFlow Medical
- Inspection Date: 2026-09-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Los Angeles District Office
- Citation Count: 2

## 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
- [FDA Inspection 916547 - 2015-02-26](https://www.keypedia.com/records/fda_inspections/reflow-medical/f52ac186-99d8-4e25-a58c-74da3634dab8)

## Related Officers

- [Investigator](https://www.keypedia.com/people/jordan-i-abel/9cdc8877-ab20-4c0c-a17e-a8534d4f13f2)

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

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b