QIAGEN Instruments AG

Form 483

Hombrechtikon, -, SwitzerlandFEI 3005621256Issued October 16, 2014

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 3005621256.

Observations1

Issue DateOctober 16, 2014

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: QIAGEN Instruments AG
Location: Hombrechtikon, -, Switzerland
FEI Number: 3005621256
Product Type: Devices
Issue Date: October 16, 2014
Country: Switzerland

Inspection History, 2013 to 2016

NAI1

VAI2

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

QIAGEN Instruments AG FDA Form 483, Hombrechtikon, October 16, 2014