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FDA Food Facility Registration Number: 13199019672
Department of Agriculture Food Permit Number: 1661836
Food Entity Number: 376617

Whether we are supporting product development, manufacturing, or testing to release, our systems are built to ensure compliance by design, not by inspection. Ours is an industry where quality, flexibility, and reliability must prevail. Across these production sectors are the customization that supports the unique needs of each customer.

Core Values:

At Ion Labs, we stay committed to our core values…quality, transparency, trust, and traceability. These steps ensure the best customer service:

Quality – We take pride in each item made, providing the highest quality products in nutrition and health supplement manufacturing.

Transparency – Our full-scale operation takes place under one roof. This model allows our company to keep consumer costs down, ensuring absolute quality throughout the process – preserving the integrity of the brand.

Trust – From product development to contract manufacturing to packaging, adherence to cGMP compliance in an FDA-registered facility has been our formula for reliability and product fulfillment.

Traceability – We create, test, produce, and ship from our Tampa Bay 150,000 sq. ft. custom facility, ensuring optimum quality control. We operate in compliance with current good manufacturing practices (cGMP) and observe FDA regulatory requirements, ensuring our FDA, cGMP, and NSF certifications.

We treat others with respect. From initial conversations with customers to delivering the final product, we aim to make every step a seamless transition from start to finish. Begin the first exchange of customer service with one of our experienced Account Executives, who will then continue the in-house dialogue from our Research & DevelopmentQuality Control, and Lab and Testing teams to our Label & PackagingShipping & Fulfillment, and Creative Services teams. Our quality first manufacturing facility has an experienced team helping with every phase of a product lifecycle.

We invite you to meet our team and experience how we are guided by our core values. Reach out to us today and we’ll demonstrate the importance of having everything under one roof philosophy.



Whether a product is required from concept, needs formulation enhancement, flavor improvement, or reverse engineering, we have the experience and supplier matrix to perform those services. Ion’s R&D department works closely with our internal quality assurance and manufacturing divisions to support product development.


These processes are performed at each step of processing, from raw material approval to in-process checks and controls to finished product approval for shipping. The Quality Unit is made up of the Quality Assurance Department and the Quality Control Department. The Quality Unit has final authority for approval or rejection of all phases of processing. It operates as a separate and distinct department of the company – this structure, in accordance with Good Manufacturing Practices, assures effective checks and balances to ensure product integrity.


Ion has decades of experience and training in the area of FDA compliant food and drug labeling rules, regulations, and laws. One of our most value-added services as a contract manufacturer is the expertise associated with our stringent label approval process. This process has saved countless Ion customers from costly and damaging legal and safety claims issues with regulatory agencies.


We offer extensive experience in international shipping and the often complex requirements associated with government-required proofs of credentials, permits, and certifications for export documentation. Ion Labs, Inc. makes available these requirements for its customers’ export needs.