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The FDA issued an import alert Friday for drugs made in Ranbaxy’s Mohali plant in northern India. On Monday the agency said it found “significant” violations of manufacturing rules, “including failure to adequately investigate manufacturing problems” during two plant inspections conducted in September and December 2012.
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Oh, wait, I thought that was the name of two people, who may have been shareholders when misleading statements were made, but I just looked it up and that’s a law firm. OK, so, I agree with daemon that it makes no sense they could even file this suit.
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