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hi Im emilita Kemper a regulatory administrator with FDA Imports as part of their efforts to ensure Food and Drug safety in the U.S market the FDA requires that facilities involved with producing processing packaging or labeling certain products for human or animal use are registered with the FDA and that those registrations are renewed on a regular basis all registrations must be renewed during the fdas appointed renewal period from October 1st to December 31st of each year regardless of when you first submitted your registration for those for knowing a medical device facility registration payment of the medical device facility user fee is required as part of the renewal process the amount of this fee changes from one year to another as announced by FDA prior to the start of the renewal season for those renewing a drug facility registration you may also be required to submit a product listing affirmation for any drug products listed in association with your facility whose listings