Cooper Cos. Says December FDA Warning Letter Resolved
PLEASANTON, Calif.—In an SEC filing dated July 10, The Cooper Cos. said that it had addressed problems which led to a warning letter from the Food and Drug Administration (FDA) in December. The FDA sent Cooper a warning letter on Dec. 5, 2011 and the company reported in its fiscal 2011 year-end report that the FDA had completed an inspection of the company's U.S. distribution center located in West Henrietta, N.Y., receiving a Form 483 with five observations and that those were related to labeling and packaging and, were not product specific. Read the article on VMail



