Import Program Tools

There are many resources available to assist you with understanding the import process for FDA-regulated products.  Below you will find links to these resources.

• Product Codes and Product Code Builder
  Ensuring that you have the correct FDA product code is an important step in the electronic import entry process. The Product Code Builder Application and Tutorial page will guide you through an easy and user-friendly selection process that will assist you in locating and building a product code. 
• FDA Data Dashboard
  The FDA Data Dashboard provides inspection, compliance and enforcement related data in a graphic format. This tool allows users to get detailed information and export the graphs and underlying data.
• Imports News & Events
  For import-related announcements, please visit our Imports News and Events page.
• Voluntary Qualified Importer Program (VQIP)
  VQIP is a voluntary, fee-based program that allows importers to receive expedited review and importation of foods into the United States if they apply, and then achieve and maintain, a high level of control over the safety and security of their supply chains. The FDA was required to establish VQIP by the FDA Food Safety Modernization Act (FSMA).
• Overview of the SUPPORT Act Provisions Related to Imports
  The SUPPORT (Substance Use-Disorder Prevention that Promotes Opioid Recovery and Treatment [SUPPORT] for Patients and Communities) Act grants FDA additional import authorities that FDA believes will meaningfully advance efforts to stop illegal and unsafe drugs from being imported into the United States.
• FEI Portal (NEW)
  Look up a FDA Establishment Identifier (FEI) based on a firm name and address or validate an address of an FEI.

Commodity Specific Resources

• Food
• Drugs
• Medical Devices
• Radiation-Emitting Products
• Biologics
• Animal and Veterinary
• Cosmetics
• Tobacco

 

Import Specific FDA Forms

• Form FDA 2877: Declaration for Imported Electronic Products Subject to Radiation Control Standards (PDF)
• Form FDA 766: Application for Authorization to Re label or to Perform Other Action of the Federal Food, Drug, and Cosmetic Act and Other Related Acts (PDF)
• All FDA Forms