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FDA Inspection 802882 — 3M Espe Dental Products

3M Espe Dental Products — FEI 2020493

The FDA completed an inspection of 3M Espe Dental Products on October 5, 2012 in Irvine, CA. 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
October 5, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 910135 (NAI Thu Jan 15 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 641481 (NAI Wed Jan 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources