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Welcome to the AgriForaging Blog
Discussing current issues in food safety & compliance



AskHACCP: Process Authority Review vs. HACCP Plan: What's the Difference and When Do You Need Each?
Food producers frequently hear terms such as Process Authority Review, Scheduled Process, HACCP Plan, Validation, Critical Control Point (CCP), and Food Safety Plan used interchangeably. As a result, many businesses assume these systems serve the same purpose or that one automatically satisfies the requirements of the other. They do not. While both are important food safety tools, they answer different questions and serve different regulatory functions. Understanding the dist
AgriForaging Compliance Services
3 days ago


FSIS Policy Book: The Label Is No Longer Just a Label
What the Updated FSIS Policy Book Signals About the Future of Meat and Poultry Labeling For years, many meat and poultry processors quietly relied on the USDA FSIS Food Standards and Labeling Policy Book as an operational reference point. It sat somewhere between guidance document, institutional memory, and field interpretation manual. Inspectors referenced it. Consultants referenced it. Label developers referenced it. Small processors often treated it as the closest thing to


Visual Only Inspection in Swine Slaughter: What FSIS Just Changed and What It Means Operationally
On May 21, 2026, USDA FSIS published a final rule titled Visual Post Mortem Inspection in Swine Slaughter Establishments. The rule becomes effective July 20, 2026, and represents a significant shift in how routine post mortem inspection will be conducted in swine slaughter establishments. At the center of the rule is a change to traditional post mortem inspection procedures in swine slaughter establishments. FSIS is removing the mandatory requirement for routine mandibular l


AskHACCP: Validation vs. Verification When Food Safety Records Stop Meaning What People Think They Mean
Some of the most vulnerable food safety systems we encounter are also the most heavily documented. The logs are there. Temperatures were recorded. pH readings were taken. Water activity checks were completed. Sanitation records were signed. Corrective actions were documented. From the outside, the system appears organized and under control. Then eventually, during an inspection, reassessment, audit, deviation review, or product investigation, a different question surfaces: Wh
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