Ivoclar Vivadent Manufacturing, Inc.

Form 483

Somerset, New Jersey, United StatesFEI 2244842Issued September 20, 2017

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 2244842.

Observations5

Issue DateSeptember 20, 2017

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Ivoclar Vivadent Manufacturing, Inc.
Location: Somerset, New Jersey, United States
FEI Number: 2244842
Product Type: Devices
Issue Date: September 20, 2017
Country: United States

Inspection History, 2009 to 2017

NAI2

VAI1

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

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Ivoclar Vivadent Manufacturing, Inc. FDA Form 483, Somerset, New Jersey, September 20, 2017