FDA Inspection 1040212 — 3M Company

3M Company — FEI 2183581

The FDA completed an inspection of 3M Company on Nov 27, 2017 in New Ulm, 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
Nov 27, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
New Ulm, MN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.