The FDA’s FSMA Section 204 traceability deadline, even though it is now postponed from January 2026 to July 2028, is fast approaching and manufacturers still relying on manual lot tracking, spreadsheets, or disconnected systems are sitting on a compliance time bomb.
A single gap in your traceability chain — one uninspected supplier record or one missing lot code — can escalate a routine audit into a full recall event that puts your brand, customer relationships, and margins in jeopardy.
In this upcoming session, we’ll break down:
- Exactly what FSMA 204 requires
- What “audit-ready” actually looks like in practice
- How modern ERP-driven traceability systems enable you to trace any ingredient from supplier, to finished product and back again, all in just a few minutes.
We’ll also walk through a real-world recall scenario, demonstrating how automated lot tracking contains scope, limits disposal costs, and protects brand reputation when it matters most.
Attendees will leave with a practical compliance-readiness checklist and a clear understanding of what it takes to move from reactive risk management to proactive, system-driven traceability.