FDA Inspection 799194 — 3M Company

3M Company — FEI 2110898

The FDA completed an inspection of 3M Company on Jul 19, 2012 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 19, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

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