FDA Inspection 1102025 — SurgiSmoke Solutions

SurgiSmoke Solutions — FEI 3008493151

The FDA completed an inspection of SurgiSmoke Solutions on August 8, 2019 in Saint Paul, MN. 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
August 8, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Paul, MN (United States)