Vygon GmbH & Co. KG

Form 483

Aachen, -, GermanyFEI 3002808464Issued January 29, 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 3002808464.

Observations2

Issue DateJanuary 29, 2015

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Vygon GmbH & Co. KG
Location: Aachen, -, Germany
FEI Number: 3002808464
Product Type: Devices
Issue Date: January 29, 2015
Country: Germany

Inspection History, 2014 to 2025

NAI2

VAI2

OAI1

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

Vygon GmbH & Co. KG FDA Form 483, Aachen, January 29, 2015