FDA Demands Recall of Applied Ozone Systems Ozone Generators, Company Refuses
12/29/2009 7:32:22 AM
Newsinferno.com -- Applied Ozone Systems, of Auburn, California has refused to recall a product that the U.S. Food & Drug Administration (FDA) says is an unapproved medical device. According to an FDA letter demanding a recall, the company allegedly claims that its AOS-1M ozone generator and AOS-1MD ozone generator devices treat cancer, AIDS, hepatitis, herpes and other infections and diseases.
comments powered by