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Suspension of ODE activities

This article was originally published in The Gray Sheet

Executive Summary

FDA plans to announce in an upcoming Federal Register notice a two- to three-week suspension of the Office of Device Evaluation's activities, along with a suspension of the office's statutory review clock, to allow for relocation of ODE offices. The move from 1390 Piccard Drive to 9200 Corporate Blvd. in Gaithersburg, Maryland is expected to take place in October ("The Gray Sheet" Aug. 15, In Brief). The notice will be similar to one that was published in 1989 when it moved from Silver Spring, Maryland to its current location ("The Gray Sheet" May 29, 1989, In Brief)

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