FDA Inspection 797869 — Goodman, Roger D.D.S.

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

The FDA completed an inspection of Goodman, Roger D.D.S. on Sep 4, 2012 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
Sep 4, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Okemos, MI (United States)

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