Thursday, September 7, 2017

FDA Warns Pfizer's Meridian Unit on EpiPen Oversight, Quality Issues

The Food and Drug Administration issued a scathing warning letter to a Pfizer Inc. unit that manufactures the emergency auto-injector EpiPen, saying the company “failed to thoroughly investigate” product failures even in cases of patients’ deaths.

from WSJ.com: US Business http://ift.tt/2gLZlR7
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