Gentian AS

Form 483

Moss, -, NorwayFEI 3006801241Issued June 21, 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 3006801241.

Observations1

Issue DateJune 21, 2012

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Gentian AS
Location: Moss, -, Norway
FEI Number: 3006801241
Product Type: Devices
Issue Date: June 21, 2012
Country: Norway

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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Gentian AS FDA Form 483, Moss, June 21, 2012