When the FDA schedules a visit to your facility with Form 482 (Notice of Inspection) and is about to audit your imported products and requests your documents, make sure you speak with us first. We are experts at guiding you through the audit process to ensure that you provide the right documentation and that the flow of your goods is not interrupted by CBP and/or FDA. When you are a KLA client, we prepare you well in advance of the audit by gathering documents and thus assuring that appropriate records are on file as required by the FSMA/FSVP rules.