FDA Inspection 1114844 — Carematix, Inc.

Carematix, Inc. — FEI 3003982635

The FDA completed an inspection of Carematix, Inc. on December 19, 2019 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
December 19, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)