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Help with registering food facilities with the FDA.

The Biannual Re-registration period for existing registered facilities is underway until December 31, 2016.  We can help - use the Contact Us tab above to send us a message and get started!  Don't delay - Time is of the essence!

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ESPANOL
The FDA Food Safety Modernization Act, signed into law on January 4, 2011, requires all domestic and foreign facilities that manufacture, process, pack or hold food for human or animal consumption in the USA to register with the FDA.

The biennial re-registration requirement has begun, and is now required in all even-numbered years.  The period for re-registrations began on October 1, 2016 and ends at midnight on December 31, 2016.  All such foreign facilities must nominate an agent with a physical presence in the USA in order to complete a new registration or to re-register their facility.
 

The role of the US Agent has changed substantially with new FDA liability requirements.  Keep your facility registration safe and up-to-date by nominating Kingbe International as your US Agent. 

In order to re-register your facility, FDA requires your original facility Registration Number and your original PIN number.  Both of these numbers were sent by FDA on the original Registration Confirmation notice to the person or organization that completed the original registration.  Many companies have the facility Registration Number but have lost or forgotten their PIN.  The FDA system will NOT generate a new PIN.  If you do not have either of these numbers, use the Contact Us tab to send us an email for assistance or instructions.

Kingbe International has been serving foreign exporters of food and beverage products as their US FDA agent since 2003.

As your FDA US agent, Kingbe International will provide the following services year-round:


  • Provide a physical presence in the USA as required by legislation.
  • Provide communication access for the FDA on a 24-hour per day, 7 days a week basis, including weekends and holidays.
  • Maintain records of all client registrations for presentation to FDA on demand.
  • Provide a communication link between the FDA and our clients.
  • Update clients on any FDA changes or updates that may impact their exports to the USA.
  • Intercede as needed to resolve particular shipment issues.
  • Translate communications or documents between English and Spanish or English and Portuguese.
  • Assist with or attend FDA facility inspections.
  • Provide consultative or preliminary facility inspections as per the Foreign Supplier Verification Program.

Call us or send us an email using the Contact US tab for terms and conditions.



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