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Re: einstock post# 687

Tuesday, 06/25/2013 8:29:54 PM

Tuesday, June 25, 2013 8:29:54 PM

Post# of 54986
Good point. It is about the Big picture where the FDA doesn't oversee. The FDA approval would only sweeten the pot. After additional readings in other articles these other rejected products were submitted under SE pathway or substantial equivalence pathway. I would imagine 22 century would full under a different category like modified risk. Appreciate the post Van!
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