FDA Inspection 1107326 — Ischenaview, Inc.

Ischenaview, Inc. — FEI 3014269683

The FDA completed an inspection of Ischenaview, Inc. on September 19, 2019 in Golden, CO. 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
September 19, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Golden, CO (United States)