March 9, 2018 / 3:42 PM / 5 months ago

BRIEF-U.S. FDA Issues Warning Letters To Duodenoscope Manufacturers, Olympus, Fujifilm And Pentax

March 9 (Reuters) - Fujifilm Holdings Corp:

* U.S. FDA SAYS ISSUED WARNING LETTERS TO DUODENOSCOPE MANUFACTURERS, OLYMPUS, FUJIFILM, PENTAX FOR FAILING TO COMPLY WITH REQUIREMENTS OF FEDERAL LAW

* U.S. FDA - AS PER FEDERAL LAW REQUIREMENTS THE MANUFACTURERS WERE TO CONDUCT POSTMARKET STUDIES TO ASSESS EFFECTIVENESS OF REPROCESSING DUODENOSCOPES

* U.S. FDA - EXPECTS OLYMPUS, FUJIFILM, PENTAX TO SUBMIT A PLAN BY MARCH 24 OUTLINING HOW THE POSTMARKET SURVEILLANCE STUDY MILESTONES WILL BE ACHIEVED Source text : [reut.rs/2Ft48lE] Further company coverage:

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