FDA Inspection 1019344 — Solventum US LLC

Solventum US LLC — FEI 3003399824

The FDA completed an inspection of Solventum US LLC on June 21, 2017 in Columbia, MO. 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
June 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Columbia, MO (United States)