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Goodman, Roger D.D.S. FDA Inspection Record

FEI 1000220754 · Inspections, Form 483s, warning letters and import refusals

Goodman, Roger D.D.S. is an FDA-inspected facility (FEI 1000220754) located in Okemos, MI, US. RegDataLab tracks 3 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jun 9, 2015: Voluntary Action Indicated (VAI)
Inspections on record
3 (1 VAI, 2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Jun 9, 2015Voluntary Action Indicated (VAI)Design changes - Lack of or Inadequate Procedures (21 CFR 820.30(i))
Lack of or inadequate procedures (21 CFR 820.100(a))
Sep 4, 2012No Action Indicated (NAI)No citations listed
Oct 8, 2010No Action Indicated (NAI)No citations listed

Facility details

Company
Goodman, Roger D.D.S.
Location
Okemos, MI (US)
Source
inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.