FDA Inspection 756134 — SleepNet Corporation

SleepNet Corporation — FEI 1222088

The FDA completed an inspection of SleepNet Corporation on December 7, 2011 in Hampton, NH. 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 7, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Hampton, NH (United States)