FDA Inspection 738912 — SurgiSmoke Solutions

SurgiSmoke Solutions — FEI 3008493151

The FDA completed an inspection of SurgiSmoke Solutions on July 27, 2011 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
July 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)