Vygon MFG, Inc.

Form 483

Dover, New Hampshire, United StatesFEI 1000120555Issued September 23, 2016

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 1000120555.

Observations2

Issue DateSeptember 23, 2016

StatusNo Warning Letter

Related Inspections6

Establishment Details

Firm: Vygon MFG, Inc.
Location: Dover, New Hampshire, United States
FEI Number: 1000120555
Product Type: Devices
Issue Date: September 23, 2016
Country: United States

Inspection History, 2009 to 2018

NAI1

VAI5

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.

Vygon MFG, Inc. FDA Form 483, Dover, New Hampshire, September 23, 2016