FDA Inspection 709948 — 3M Company

3M Company — FEI 2183581

The FDA completed an inspection of 3M Company on Jan 27, 2011 in New Ulm, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
New Ulm, MN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
54621 CFR 820.75(a)Lack of or inadequate process validation

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