FDA Inspection 853465 — The Snore Reliever Company LLC

The Snore Reliever Company LLC — FEI 3008583502

The FDA completed an inspection of The Snore Reliever Company LLC on October 25, 2013 in Largo, FL. 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 25, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Largo, FL (United States)