PITTSBURGH, Aug. 13 /PRNewswire-FirstCall/ -- Mylan Inc. today announced that the U.S. Food and Drug Administration (FDA) has released its official and final report regarding the agency’s review of allegations made in a July newspaper article concerning the company’s Morgantown, W.Va., manufacturing facility. The newspaper article, which included unfounded and highly inaccurate allegations, was based on improperly obtained documents, uninformed third-party commentary and anonymous sources. The final FDA report closes the inspection with no deficiencies found and no FDA “483" issued.
“Mylan’s manufacturing facilities -- especially our plant in Morgantown -- have always represented the gold standard when it comes to quality. Without ever getting complacent, our entire management team and all of our employees continue to demonstrate an unyielding commitment to sustain the highest of quality standards. I would like to thank all of our employees for their continued hard work and execution, and I am pleased that this investigation is formally behind us.”
Mylan Inc.
