FDA Inspection 684056 — 3M Company

3M Company — FEI 2110898

The FDA completed an inspection of 3M Company on August 16, 2010 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
August 16, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)