DMG America LLC dba Goldsmith & Revere, Inc.

Form 483

Englewood, New Jersey, United StatesFEI 2244812Issued January 29, 2013

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 2244812.

Observations3

Issue DateJanuary 29, 2013

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: DMG America LLC dba Goldsmith & Revere, Inc.
Location: Englewood, New Jersey, United States
FEI Number: 2244812
Product Type: Devices
Issue Date: January 29, 2013
Country: United States

Inspection History, 2010 to 2015

NAI2

VAI3

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

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DMG America LLC dba Goldsmith & Revere, Inc. FDA Form 483, Englewood, New Jersey, January 29, 2013