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FDA Inspection 567002 — SurgiSmoke Solutions

SurgiSmoke Solutions — FEI 3008493151

The FDA completed an inspection of SurgiSmoke Solutions on February 13, 2009 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
February 13, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)

Facility

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FDA data resources