Compliance
FSMA 204, audits, and electronic batch records. What the rules actually ask you to capture, where paper and spreadsheets tend to fall short of it, and how to find out whether your records would hold up before an inspector does.
FSMA 204 Section 204(d) Receiving & Transformation KDEs: A Step-by-Step Guide for Food Processors
FDA FSMA 204 mandates capturing specific Key Data Elements (KDEs) for every Critical Tracking Event (CTE) across high-risk foods. Learn how food processors digitize incoming raw material receiving, transformation work orders, and 24-hour trace spreadsheets.
Metal Contamination & Foreign Body Recalls: Implementing Digital Magnet & X-Ray Inspection Logs for SQF Audits
Foreign body contamination remains one of the top causes of FDA physical hazard recalls. Learn how digitizing CCP metal detection logs and automated lot hold prevents costly product withdrawals.
Preventing Undeclared Allergen Recalls: How Batch Manufacturers Automate Line Clearance & Changeover
Why undeclared allergens remain a leading cause of food recalls in the US and UK, and the line clearance, cleaning verification and packaging checks that prevent them.
FSMA 204 Critical Tracking Events: How Food Manufacturers Master CTE & KDE Recordkeeping
The Key Data Elements FSMA 204 requires at receiving, transformation and shipping, the mistakes that break a trace, and how to answer an FDA records request within 24 hours.
Have a question these do not answer?
We would rather talk through your actual situation than send you more reading. Tell us what you are wrestling with.
Talk to an Expert