FDA Warning Letter — Somnowell, Inc.

Case 493804 — FEI 3011669995

The FDA took a Warning Letter action against Somnowell, Inc. on May 12, 2016 (Bellevue, TN). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Somnowell, Inc.
Date
May 12, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Bellevue, TN (United States)