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FDA Inspection 803728 — Rite-dent Manufacturing Corp.

Rite-dent Manufacturing Corp. — FEI 3003064146

The FDA completed an inspection of Rite-dent Manufacturing Corp. on August 28, 2012 in Hialeah, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 28, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hialeah, FL (United States)

Facility

Other inspections at this facility

  • 698163 (OAI Tue Nov 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 670603 (OAI Thu Jul 08 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 654426 (NAI Tue Mar 23 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

  • Seizure (126211) (Wed Jan 05 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources