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When you receive a Notice of Action, you are entitled to various options, including An informal hearing to provide testimony regarding the admissibility of the product Submission of evidence that the product is compliant Evidence will include either a label review or laboratory analysis, depending on the specifics of the refusal Failure to submit evidence or a plan to bring the product into compliance results in only two options: Destroy the product under FDA and CBP supervision Incurs added cost since FDA or CBP will send personnel to supervise Export the product under FDA and CBP supervision If you receive a Notice of Action, its important to review it and respond immediately, as we explain in this post

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