Law360, New York (May 29, 2012, 8:46 PM ET) -- A Johnson & Johnson unit has failed to adequately respond to some of the over 200 complaints it has received about its K-Y vaginal moisturizer products, according to a U.S. Food and Drug Administration warning letter made public Tuesday.
In a letter dated May 22, the FDA warned McNeil-PPC Inc. that a winter inspection of the pharmaceutical company had revealed that the manufacturing, packing and storage of several of its K-Y products, as well as tampons, floss and eye drops, did not conform with manufacturing practice...
FDA Warns J&J It Can't Slip Away From K-Y Complaints
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