Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3008789872.
Observations2
Issue DateSeptember 21, 2026
StatusNo Warning Letter
Related Inspections4
Establishment Details
Firm
ReFlow Medical
Location
San Clemente, California, United States
FEI Number
3008789872
Product Type
Devices
Issue Date
September 21, 2026
Country
United States
Inspection History, 2015 to 2026
NAI3
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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