FDA Warning Letter — THEROZONE USA, INC.

Case 180272 — FEI 3007025733

The FDA took a Warning Letter action against THEROZONE USA, INC. on August 11, 2011 (Santa Monica, CA). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
THEROZONE USA, INC.
Date
August 11, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Santa Monica, CA (United States)