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FDA Inspection 735900 — Caerus Corp

Caerus Corp — FEI 3008216220

The FDA completed an inspection of Caerus Corp on July 1, 2011 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
July 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Blaine, MN (United States)

Facility

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