FDA Inspection 963097 — Eos Imaging, Inc.

Eos Imaging, Inc. — FEI 3008632827

The FDA completed an inspection of Eos Imaging, Inc. on Mar 17, 2016 in Saint Paul, MN. 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
Mar 17, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Saint Paul, MN (United States)