FDA Inspection 1072151 — Caerus Corp

Caerus Corp — FEI 3008216220

The FDA completed an inspection of Caerus Corp on October 10, 2018 in Blaine, MN. 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
October 10, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Blaine, MN (United States)