FDA Inspection 676068 — 3M, Company 3M ESPE Dental Products

3M, Company 3M ESPE Dental Products — FEI 1000118617

The FDA completed an inspection of 3M, Company 3M ESPE Dental Products on August 12, 2010 in Ardmore, OK. 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 12, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ardmore, OK (United States)