Belimed AG

Form 483

Sulgen, -, SwitzerlandFEI 3003927243Issued August 10, 2012

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 3003927243.

Observations7

Issue DateAugust 10, 2012

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Belimed AG
Location: Sulgen, -, Switzerland
FEI Number: 3003927243
Product Type: Devices
Issue Date: August 10, 2012
Country: Switzerland

Inspection History, 2012 to 2015

NAI1

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Belimed AG FDA Form 483, Sulgen, August 10, 2012