Vygon MFG, Inc.

Form 483FOIA Uncovered

Dover, New Hampshire, United StatesFEI 1000120555Issued May 21, 2018

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.

Observations1

Issue DateMay 21, 2018

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: May 21, 2018
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

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Vygon MFG, Inc. FDA Form 483, Dover, New Hampshire, May 21, 2018