Goodman, Roger D.D.S.

Form 483

Okemos, Michigan, United StatesFEI 1000220754Issued June 09, 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 1000220754.

Observations2

Issue DateJune 09, 2015

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Goodman, Roger D.D.S.
Location: Okemos, Michigan, United States
FEI Number: 1000220754
Product Type: Devices
Issue Date: June 09, 2015
Country: United States

Inspection History, 2010 to 2015

NAI2

VAI1

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

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Goodman, Roger D.D.S. FDA Form 483, Okemos, Michigan, June 9, 2015