FDA Inspection 1305822 - Reflow Medical - March 05, 2026

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Record Details

This FDA Inspection record concerns Reflow Medical, with an inspection on March 5, 2026, issued by the Los Angeles District Office, covering medical devices & rad health.

Company: Reflow Medical
Inspection Date: March 5, 2026
Product Type: Medical Devices & Rad Health
Office: Los Angeles District Office

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ID · cf0d0a9e-1ef2-4b91-8afe-2b0b69bab544

Violation Codes1

ISO 13485:2016 Clause 7.4.1

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