Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3007025733.
Observations4
Issue DateMarch 16, 2011
StatusNo Warning Letter
Related Inspections2
Establishment Details
Firm
THEROZONE USA, INC.
Location
Santa Monica, California, United States
FEI Number
3007025733
Product Type
Devices
Issue Date
March 16, 2011
Country
United States
Inspection History, 2011 to 2012
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.