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FDA Inspection 799456 — 3M Espe Dental Products

3M Espe Dental Products — FEI 3005174370

The FDA completed an inspection of 3M Espe Dental Products on September 20, 2012 in Saint Paul, MN. 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
September 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1046452 (NAI Wed Mar 07 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 872250 (NAI Wed Mar 12 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 698056 (VAI Fri Nov 19 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 579363 (VAI Fri Mar 13 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources