FDA Inspection 830531 — SurgiMark, Inc.

SurgiMark, Inc. — FEI 3023415

The FDA completed an inspection of SurgiMark, Inc. on May 2, 2013 in Yakima, WA. 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
May 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Yakima, WA (United States)