FDA EIR - ADM Southport - June 13, 2023

An FDA inspection was conducted at ADM Southport, located at 1730 E Moore St, Southport, NC, from June 13 to June 15, 2023. This routine inspection aimed to assess the facility's compliance with the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Food for Human Regulations, specifically 21 CFR Part 117, subparts A, B, and F. The scope covered various operational aspects including pest control, plant and grounds maintenance, employee training, receipt and distribution of finished goods, hazard analysis, food safety plans, recall procedures, and consumer complaint handling. Crucially, the inspection concluded with no objectionable conditions noted. No FDA Form 483, Inspectional Observations, was issued, and no samples were collected. The inspection was classified as 'No Action Indicated' (NAI), signifying full compliance and indicating that no corrective or follow-up actions are required from the company.