FDA Inspection 680133 — Eyebobs Inc.

Eyebobs Inc. — FEI 3003433048

The FDA completed an inspection of Eyebobs Inc. on Sep 14, 2010 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 14, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)