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Sunday, 06/14/2015 6:23:10 PM

Sunday, June 14, 2015 6:23:10 PM

Post# of 1825
FDA is fixing to close NEPH down
However, failure to promptly address the issues raised in the Warning Letter to the FDA’s satisfaction or to comply with U.S. medical device regulatory requirements in general could result in regulatory action being initiated by the FDA. These actions could include, among other things, delays in approval of any FDA applications, product seizures, injunctions and civil monetary penalties. Any such actions could disrupt our ongoing business and operations and potentially have a material adverse impact on our financial condition and operating results.

Everything I say and write is my opinion and my opinion only. Do your own due diligence when investing

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