FDA Inspection 861805 — VasSol, Inc.

VasSol, Inc. — FEI 3003494057

The FDA completed an inspection of VasSol, Inc. on Jan 9, 2014 in River Forest, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 9, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
River Forest, IL (United States)