FDA Inspection 1153967 — Qlarity Imaging

Qlarity Imaging — FEI 3015529351

The FDA completed an inspection of Qlarity Imaging on September 30, 2021 in Chicago, IL. 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 30, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)