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Info on Device Electronic Registration Sent to OMB

05/07/2008

Federal Register Notice: FDA’s proposed collection of information on the requirements that device establishments must submit registration and listing information by electronic means using FDA Form 3673 unless they have a waiver, has been submitted to the Office of Management and Budget (OMB) for emergency processing under the Paperwork Reduction Act of 1995. To view this notice, click here.

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