I will assist with fda food facility registration and US agent coordination
About this gig
Need help preparing your FDA food facility registration for the U.S. market?
I assist food manufacturers, processors, packers, storage facilities, and international food exporters with organized FDA food facility registration support.
My services include:
- Initial registration information preparation
- Facility details and UFI/DUNS checks
- Registration document checklist
- U.S. Agent coordination for foreign facilities
- Review of information before authorized submission
- Registration record documentation
Choose your package:
Basic: A registration information checklist for one facility.
Standard: Preparation and review of registration information for one facility.
Premium: Expanded preparation, document checks, and U.S. Agent coordination where available.
I prioritize clear communication, confidentiality, and careful information handling.
Please message me before ordering if you have multiple facilities, a complex ownership structure, or an existing registration.
Important: FDA registration is not FDA approval or a product endorsement. Government requirements, eligibility, and submission outcomes are determined by the FDA.
Get to know Lana Hook
FDA Registration and Compliance
- FromUnited States
- Member sinceOct 2026
Languages
English
FAQ
Who needs FDA food facility registration?
Facilities that manufacture, process, pack, or hold food for U.S. consumption may need registration, subject to applicable exemptions.
Can you assist international food exporters?
Yes. I can help organize facility information and coordinate U.S. Agent arrangements where available.
Is FDA registration the same as FDA approval?
No. Registration does not mean the FDA has approved a facility or its products.
What information do you need to begin?
Facility details, business information, product or activity categories, and relevant existing registration information if available.
Can you guarantee successful registration?
No. I provide careful preparation and authorized submission support, but the FDA determines regulatory outcomes.

