FDA 483 - Best Foods NJ, Inc. - September 18, 2025

An FDA inspection was conducted at a food repackaging facility, identified only as 'your firm' in the document, from September 15 to September 18, 2025. The inspection revealed a significant observation: the company did not possess a written food safety plan or a written hazard analysis for any of the products it repackages. Specifically, this included dried whole black lentils (urad daal), dried split red lentils (masoor dal), and previously, ready-to-eat (RTE) spices. The firm acknowledged repackaging bulk quantities into smaller, branded plastic bags for a single customer, with these operations reportedly taking place on a table in a warehouse area. Furthermore, the facility lacked an environmental monitoring program, which is essential for verifying the effectiveness of sanitation controls. These findings were detailed in an FDA Form 483, issued under Section 704(b) of the Federal Food, Drug, and Cosmetic Act. This document serves as an inspectional observation and not a final determination of compliance. The company is expected to address these noted conditions, either by discussing objections or submitting plans for corrective actions, to ensure adherence to regulatory standards.