Global Import Agent

FSVP Agent Services & Assessments

Under FSVP, the importer is the U.S. owner or consignee of the food at entry. If there isn't one, the importer is the foreign owner's U.S. agent or representative, confirmed by a signed statement of consent (21 CFR 1.500). That importer must verify its foreign suppliers. Global Import Agent can act as your FSVP agent.

· By the Global Import Agent team
Overview

Who is the FSVP importer?

The importer carries the supplier-verification responsibility under FSVP.

  • The importer is the U.S. owner or consignee at entry, or, if there isn't one, the foreign owner's U.S. agent or representative confirmed by signed consent (21 CFR 1.500).
  • FSVP records must generally be kept for at least 2 years (21 CFR 1.510(c)).
  • When FDA requests records held offsite, they must be provided within 24 hours (21 CFR 1.510(b)(2)).
Cargo containers moving through an international port

Acting as Your Designated FSVP Agent

Foreign suppliers shipping food to the US must designate a US-based FSVP Agent, and we act as yours, managing supplier compliance, records and FDA communication.

  • Serving as your official FSVP Agent for compliance and audits
  • Handling FDA enquiries and supplier verification documents
  • Ongoing monitoring and reporting of foreign supplier compliance
  • Support for FDA inspections and enforcement actions

Supplier Compliance Assessments

FSVP requires US importers to verify that foreign suppliers follow FDA safety standards, and we assess your suppliers before importation.

  • Reviewing supplier food safety and hazard control plans
  • Verifying compliance with GMP and HACCP standards
  • Ensuring proper record-keeping and documentation for FDA audits
  • Evaluating supplier corrective action plans (CAPs) for previous violations
Product documentation being reviewed for compliance
Food & Beverage

FSVP Agent & Assessments

Product Assessments for FDA Compliance

Before you import food, beverages or dietary supplements, we assess each product against FDA standards.

  • Ingredient safety and allergen assessment
  • Label review for compliance with FDA food labelling laws
  • Evaluation of food safety risks and hazards
  • Verification of claims (e.g., organic, non-GMO) for regulatory approval

Import Documentation & FDA Prior Notice Support

Proper documentation helps avoid shipment delays and FDA detentions, so we check your import documents against FSVP and Prior Notice requirements.

  • Full FDA Prior Notice submission assistance
  • Review of bill of lading, commercial invoices, and packing lists
  • Verification of supplier food facility registration status
  • Assistance with Customs and Border Protection (CBP) coordination

Corrective Actions for FDA Non-Compliance

If your foreign supplier has been cited for FSVP violations or FDA import refusals, we help you put corrective actions in place and resume importing.

  • Developing and submitting Corrective Action Plans (CAPs) to the FDA
  • Working with foreign suppliers to improve food safety programmes
  • Assisting with FDA re-inspection and compliance audits
  • Re-evaluating supplier verification programmes for ongoing compliance

Foreign Facility Registration Services

We handle the full facility registration process for food, beverage, dietary supplement and cosmetic facilities.

  • Preparing and submitting your FDA facility registration
  • Ensuring accuracy in facility details to avoid delays or errors
  • Managing renewals during the biennial renewal period
  • DUNS confirmation and matching for all international countries

FSVP Programme Development and Records

We build and maintain the FSVP programme itself, so verification is documented and ready for FDA inspection.

  • Hazard analysis for each food and foreign supplier combination, covering biological, chemical, physical and radiological hazards
  • Verification activities before importing and at appropriate intervals afterwards
  • FSVP records kept for at least two years (21 CFR 1.510)
  • Periodic programme reviews and corrective actions when a supplier falls short
  • Coordination with customs clearance and freight forwarding

Ongoing compliance support

  • Time-Saving

    We manage supplier verification documents and FDA enquiries, so your team doesn't have to.

  • Regulatory Assurance

    Ongoing monitoring keeps your foreign suppliers aligned with FSVP requirements under FSMA.

  • Peace of Mind

    Audit-ready records and inspection support reduce the risk of detentions and enforcement action.

What you'll need

FSVP rests on supplier evidence, so gather these before appointing an agent.

  • Supplier food safety plansHazard control plans from each foreign supplier.
  • GMP or HACCP evidenceProof your suppliers work to recognised standards.
  • Supplier recordsDocumentation kept ready for FDA audits.
  • Shipping documentsBills of lading, commercial invoices and packing lists.
  • Supplier registration statusConfirmation each supplier's food facility is registered.
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Official sources

Related services: FDA US Agent service

Client feedback

Trusted support, in our clients’ own words.

“Global Import Agent have successfully worked with me to land product in the U.S and remain compliant for FDA regulations. I'm really happy with their response times, and easy to use tech platform that facilitates the process.”
Jane MckayAstute Beverages
Frequently asked questions

FSVP Agent & Assessments

Requirements vary by product and destination. These answers outline the starting point for the questions we receive most often.

Ask our team

Who needs to comply with FSVP?

FSVP applies to most U.S. food importers, except for those importing from suppliers with certain exemptions (e.g., USDA-regulated meat, eggs, and poultry). If you import human or animal food, you likely need to comply.

Do I need an FSVP Agent if I’m a foreign supplier?

Yes. If you’re a foreign supplier shipping food to the U.S., you must appoint a U.S.-based FSVP Agent to handle FDA communications and compliance on your behalf.

What happens if I don’t comply with FSVP?

Non-compliance can result in:

  • Import detentions and holds
  • Warning letters and penalties from the FDA
  • Loss of import privileges and inability to bring products into the U.S.

How long does an FSVP product assessment take?

A typical product compliance assessment takes 5–10 business days, depending on the complexity of the product and regulatory review needs. Expedited reviews are available.

How do I verify if my supplier meets FSVP requirements?

FSVP requires U.S. importers to verify that their foreign suppliers: - Follow Good Manufacturing Practices (GMP) - Have a hazard analysis and risk control plan - Maintain proper documentation and records

We conduct FSVP compliance audits to help you verify supplier compliance.

What if my supplier is already FDA-registered? Do I still need FSVP compliance?

Yes. FDA registration is not the same as FSVP compliance. Even if a supplier is FDA-registered, you must still verify that their manufacturing, safety, and hazard control processes meet U.S. requirements.

How often must FSVP supplier verification activities be conducted?

Verification activities must occur before importing from a supplier and periodically thereafter based on risk assessment. Higher-risk foods or suppliers may need more frequent verification. We establish appropriate verification schedules based on hazard analysis and FDA guidance for your specific products.

What documentation is required for FSVP compliance and FDA inspections?

FSVP records must include hazard analyses, supplier verification procedures, verification activity records, and corrective action documentation. All records must be maintained for at least two years and available for FDA inspection. We manage complete documentation systems ensuring inspection readiness and proper record retention compliance.

Discuss your requirements

Talk through your product and target market with our team.

Consultation

Tell us what you need to import.

Share your product, target market and compliance question. A member of our team will respond promptly.

Scope your product and target market
Identify the applicable regulatory route
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