FDA Inspection 952580 — 3M Company

3M Company — FEI 1510709

The FDA completed an inspection of 3M Company on November 6, 2015 in Milford, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 6, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Milford, OH (United States)

Citations

IDCFRDescription
73121 CFR 803.50(a)(1)Report of Death or Serious Injury