The Food and Drug Administration (FDA) carried out an inspection at Keurig Dr. Pepper in Goodlettsville on Feb. 26, targeting foodborne biological hazards, FDA data shows.
The inspection concluded with no corrective action required for Keurig Dr. Pepper’s operational management.
The FDA conducts regular inspections of facilities nationwide to ensure workplaces and products comply with FDA-regulated standards and regulations designed to promote public health. The agency releases inspection results to the public.
The FDA website states that the agency is primarily charged with overseeing the safety and quality of human and animal drugs, biological products, medical devices, and tobacco products.
Information in this article was sourced from the U.S. Food and Drug Administration. The primary data is available here.
