How Global Import Agent Protects Your US Food Imports
FDA import enforcement can expose gaps in FSVP records, facility registration and entry documentation. Our FDA specialists provide end-to-end compliance management, from Foreign Supplier Verification Programs (FSVP) under 21 CFR 1. 500-1. 514 to mandatory US Agent services and facility registration under 21 CFR 1. 226-1. 243.
We prevent the regulatory gaps that trigger Detention Without Physical Examination, managing everything from hazard analysis documentation to Prior Notice submissions under 21 CFR 1. 276-1. 285. Our dedicated account managers ensure your brand stays compliant as FDA enforcement intensifies, with unannounced virtual inspections now requiring just 72-hour notice.
Complete Foreign Supplier Verification Program management, hazard analysis, and documentation under 21 CFR 1. 500-1.
- 514
- Mandatory US Agent services for food facility registration, FDA communications, and emergency contact requirements
- FDA Compliance Auditing – Label reviews, nutritional facts panel compliance, and preventive controls verification under 21 CFR 117
Why FDA import alerts matter more in 2026
The FDA’s enforcement shift follows high-profile foodborne illness outbreaks linked to imported products and increased Congressional funding for the agency’s import safety programme. Preventive Controls and nutritional labelling failures can trigger enforcement action and disrupt imports.
UK food brands face particular scrutiny due to post-Brexit regulatory divergence, with facility registration violations triggering automatic import alerts under new enforcement protocols. The FDA’s enhanced data analytics now identify non-compliant importers before products reach US borders, making proactive compliance essential rather than reactive damage control.
- Import alerts remain a material risk for non-compliant importers
- FSVP violations are a recurring import-alert issue
- Detention can create substantial storage, testing and legal costs
- UK exporters should be prepared for inspection
- FDA may request records during remote regulatory assessments
What We Arrange And Manage End-To-End
1) FDA Facility Registration & US Agent Setup
We complete mandatory food facility registration under 21 CFR 1. 226-1. 243 and establish compliant US Agent services.
- Bioterrorism Act registration with unique facility number
- US Agent designation for FDA communications
- Biennial registration renewal management
2) Foreign Supplier Verification Program (FSVP)
Our FSVP agents manage complete supplier verification under 21 CFR 1. 500-1. 514, preventing gaps that can trigger import alerts.
- Hazard analysis and risk evaluation
- Supplier verification activities and documentation
- Corrective action procedures
3) Label Review & Nutritional Compliance
We verify labels meet FDA requirements under 21 CFR 101, preventing non-compliance that can delay entry.
4) Prior Notice & Import Documentation
Complete Prior Notice submissions under 21 CFR 1. 276-1. 285 and import documentation management to prevent border delays.
5) Ongoing Compliance Monitoring
Continuous monitoring of FDA enforcement updates, import alert status, and supplier compliance to maintain border clearance.
Complete FDA Import Compliance Management
FSVP Agent Services
Complete Foreign Supplier Verification Program management under 21 CFR 1. 500-1. 514 with dedicated compliance documentation.
US Agent Registration
Mandatory US Agent designation for FDA communications, facility registration, and emergency contact requirements.
FDA Facility Registration
Food facility registration under Bioterrorism Act with biennial renewal management and compliance tracking.
Label & Nutritional Review
FDA label compliance verification under 21 CFR 101 to prevent detention-triggering violations.
Prior Notice Management
Automated Prior Notice submissions under 21 CFR 1. 276-1. 285 with shipment tracking and clearance confirmation.
Import Alert Prevention
Proactive compliance monitoring and corrective action to prevent the violations that trigger FDA import alerts.
What Is FDA FSVP Agent Service?
The Foreign Supplier Verification Program (FSVP) under 21 CFR 1. 500-1. 514 requires UK food importers to verify that foreign suppliers meet FDA safety standards equivalent to US preventive controls regulations. Proper FSVP implementation is critical for maintaining US market access.
Our FSVP Agent service provides the mandatory hazard analysis, supplier verification activities, and corrective action procedures required under FSMA. We maintain comprehensive documentation, manage supplier audits, and ensure ongoing compliance as FDA enforcement intensifies with FDA requests for records and remote regulatory assessments. FSVP compliance requirements:
- Hazard analysis for each imported food
- Supplier verification activities and documentation
- Risk-based supplier evaluation procedures
- Corrective action plans for non-compliance
- Records maintenance for FDA inspection
Our FSVP management process:
- Initial hazard analysis and risk evaluation
- Supplier verification programme design
- Documentation system implementation
- Ongoing compliance monitoring
- FDA inspection support and defence
Deep understanding of 2026 enforcement trends, with specialists tracking import alerts and evolving compliance requirements. We know what triggers FDA attention and how to prevent costly violations. Complete FSVP Agent, US Agent, and facility registration services under one roof, eliminating the coordination gaps that cause compliance failures.
Dedicated account managers support service delivery. Our proactive compliance approach reduces exposure to detention, storage fees and lost revenue. We’ve helped hundreds of UK food brands maintain smooth US border clearance.
Our service: FDA detention assistance