Medion Grifols Diagnostics AG

Form 483

Dudingen, -, SwitzerlandFEI 3002806769Issued July 30, 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 3002806769.

Observations1

Issue DateJuly 30, 2015

StatusNo Warning Letter

Related Inspections9

Establishment Details

Firm: Medion Grifols Diagnostics AG
Location: Dudingen, -, Switzerland
FEI Number: 3002806769
Product Type: Devices
Issue Date: July 30, 2015
Country: Switzerland

Inspection History, 2009 to 2026

NAI2

VAI7

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

Act on This Form 483

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Medion Grifols Diagnostics AG FDA Form 483, Dudingen, July 30, 2015