Key word in your question is 'satisfy', meaning - will the FDA be satisfied with Cerezyme and Fabrazyme that were produced before reinspection? I think it will cause the reinspection is probably more about the manufacturing issue detailed in a warning letter that was issued in Feb and not about the viral contamination. Key question is - when. Of course GENZ will eventually get these issues taken care of, but meanwhile, they are losing time, money, and credibility and competitors are enjoying a tailwind.