Euromi S.A.

Form 483

Dison, -, BelgiumFEI 3007697975Issued January 15, 2015

View FDA's Record for This Firm

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 3007697975.

Observations14

Issue DateJanuary 15, 2015

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Euromi S.A.
Location: Dison, -, Belgium
FEI Number: 3007697975
Product Type: Devices
Issue Date: January 15, 2015
Country: Belgium

Inspection History, 2015 to 2025

VAI1

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Euromi S.A. FDA Form 483, Dison, January 15, 2015