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FDA Inspection 698056 — 3M Espe Dental Products

3M Espe Dental Products — FEI 3005174370

The FDA completed an inspection of 3M Espe Dental Products on November 19, 2010 in Saint Paul, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 19, 2010
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
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))
  • 799456 (NAI Thu Sep 20 2012 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