This is a legal form that was released by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration on September 1, 2017 and used country-wide. As of today, no separate filing guidelines for the form are provided by the issuing department.
Q: What is Form FDA 482d?
A: Form FDA 482d is a Request for FSVP Records.
Q: What does FSVP stand for?
A: FSVP stands for Foreign Supplier Verification Program.
Q: Who is required to submit Form FDA 482d?
A: Importers subject to the FSVP regulation are required to submit Form FDA 482d.
Q: What is the purpose of Form FDA 482d?
A: The purpose of Form FDA 482d is to request and review records related to the FSVP, as part of the FDA's compliance activities.
Q: What information is included in Form FDA 482d?
A: Form FDA 482d includes details such as the importer's name, address, contact information, and the specific records being requested.
Q: How can Form FDA 482d be submitted?
A: Form FDA 482d can be submitted electronically or through other means specified by the FDA.
Q: What happens after Form FDA 482d is submitted?
A: After Form FDA 482d is submitted, the FDA may review the requested records to assess compliance with the FSVP regulation.
Q: Are there any fees associated with Form FDA 482d?
A: Currently, there are no fees associated with submitting Form FDA 482d.
Form Details:
Download a fillable version of Form FDA482d by clicking the link below or browse more documents and templates provided by the U.S. Department of Health and Human Services - U.S. Food and Drug Administration.