FDA Inspection 682781 — Goodman, Roger D.D.S.

Goodman, Roger D.D.S. — FEI 1000220754

The FDA completed an inspection of Goodman, Roger D.D.S. on Oct 8, 2010 in Okemos, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Oct 8, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Okemos, MI (United States)

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