The U.S. Food and Drug Administration recently announced that routine inspections to verify compliance with the Intentional Adulteration (IA) rule will begin in March 2020. The Food Safety and Modernization Act (FSMA) final rule on intentional adulteration is designed to address hazards that may be intentionally introduced to foods, including by acts of terrorism, with the intent to cause wide-spread harm to public health.
Unlike the other FSMA rules that address specific foods or hazards, the IA rule requires the food industry to implement risk-reducing strategies for processes in food facilities that are significantly vulnerable to intentional adulteration. Food facilities covered by the rule will be required to develop and implement a food defense plan that identifies vulnerabilities and mitigation strategies for those vulnerabilities.
These facilities will then be required to ensure that the mitigation strategies are working. The first compliance date arrives in July 2019. The FDA has heard from stakeholders that due to the novel nature of the IA rule and its requirements, they believe more time is needed to develop a fully compliant food defense plan.
The FDA says it is working to provide resources, including the final portion of draft guidance. It feels that keeping the compliance dates ensures that the industry will put in place measures that protect public health while the agency makes additional guidance and resources available.
More information about the upcoming compliance date, the recently released draft guidance, and other resources is available in an updated conversation piece featuring FDA food defense experts Ryan Newkirk and Jon Woody.
