Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3007697975.
Observations5
Issue DateJuly 31, 2025
StatusNo Warning Letter
Establishment TypeMedical Device Manufacturer
Related Inspections2
Establishment Details
Firm
Euromi S.A.
Location
Dison, Belgium
FEI Number
3007697975
Establishment Type
Medical Device Manufacturer
Product Type
Devices
Issue Date
July 31, 2025
Country
Belgium
Inspection History, 2015 to 2025
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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