FDA Inspection 979173 — SleepNet Corporation

SleepNet Corporation — FEI 1222088

The FDA completed an inspection of SleepNet Corporation on July 18, 2016 in Hampton, NH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 18, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Hampton, NH (United States)

Citations

IDCFRDescription
368221 CFR 820.70(d)Implementing Personnel Procedures, Health, Cleanliness.