Articles & Perspectives
What Is Asset Reliability Consulting for Food Plants?
5 minute read
5 minute read
Food safety programs rarely fail all at once. More often, they begin to break down through small, recurring gaps: incomplete records, inconsistent sanitation practices, overdue corrective actions, weak training, or processes that vary from one shift or facility to another.
These warning signs can be easy to dismiss when production is moving and audits occur only every few years. But over time, small weaknesses can create larger food safety, compliance, and operational risks.
The stakes are significant. The Centers for Disease Control and Prevention (CDC) estimates that 48 million people in the U.S. get sick from foodborne illnesses each year, resulting in 128,000 hospitalizations and 3,000 deaths.
For food and beverage manufacturers, recognizing the early signs of a struggling food safety program can help prevent those weaknesses from becoming bigger incidents.

A food safety program may be breaking down when processes look effective on paper but become increasingly difficult to follow through on the plant floor. Common warning signs include:
When the same issue appears across multiple internal, customer, or regulatory audits, the problem may extend beyond the original finding.
Repeat observations can indicate that corrective actions are addressing symptoms instead of root causes. For example, retraining an employee may temporarily fix a procedural deviation, but it will not solve unclear work instructions, poor process design, inadequate staffing, or a lack of accountability.
Repeat audit findings are very common in food manufacturing. Many companies implement band aid solutions, and the problems creep back up eventually. A strong corrective and preventive action process should not only close findings, but it should also reduce the likelihood that they return.
Sanitation programs often provide some of the earliest indications that food safety controls are weakening.
Procedures may differ by shift, master Sanitation Schedules may not reflect what’s happening on the floor, Clean-in-Place (CIP) processes may not have been recently validated, and environmental monitoring results may reveal recurring positives without a clear escalation process.
When sanitation depends primarily on tribal knowledge rather than documented, validated procedures, risk increases when experienced employees leave, production schedules change, or new products and equipment are introduced.
Related Case Study: Sanitation System Overhaul for a New Production Plant

Documentation should provide evidence that food safety controls are being performed consistently. When records are incomplete, difficult to locate, or maintained differently across facilities, leaders lose visibility into whether the program is functioning as designed.
This becomes particularly important for traceability. FDA’s Food Traceability Rule requires organizations handling foods on the Food Traceability List to maintain specific Key Data Elements associated with Critical Tracking Events. When required during certain situations, covered entities must be capable of providing relevant information to the FDA within 24 hours or another reasonable agreed-upon timeframe.
The inability to quickly locate records poses a risk for manufacturers’ ability to comply with the Food Traceability Rule, plus any other reason documentation may be needed for audits.
Documentation is the biggest cause of failed food safety audits. There’s a saying that “If it’s not documented, it didn’t happen.” However, consistent documentation is still a struggle for many food and beverage manufacturers.
Written procedures only work when employees understand and consistently follow them.
One way to test this is by asking operators why a particular control exists, what should happen when a limit is exceeded, or who owns the next step when an issue occurs. If answers vary significantly, the organization may have a training or food safety culture problem.
Training should go beyond completion records. Effective programs reinforce expectations, confirm competency, and ensure employees understand their role in preventing food safety risks.
73% of food manufacturing companies reported that employees do not consistently follow established protocols despite training efforts.

The goal should not be to fix each problem independently. Manufacturers should look for patterns across sanitation, training, documentation, environmental monitoring, corrective actions, audits, and plant-level execution.
A food safety program assessment can help determine whether gaps are isolated or symptoms of broader issues. This may include reviewing:
A strong food safety program is not defined by the absence of problems. It’s defined by an organization’s ability to identify risks early, address root causes, standardize effective practices, and continuously improve.
For manufacturers seeing repeated findings, inconsistent execution, documentation gaps, or other warning signs, an objective assessment can provide visibility into where the program is beginning to break down and what should be prioritized before those gaps become larger operational, regulatory, or food safety issues.
Common warning signs include repeat audit findings, inconsistent sanitation practices, incomplete documentation, overdue corrective actions, recurring environmental monitoring issues, and employees who cannot clearly explain food safety procedures.
Effective food safety training goes beyond completion records. Employees should be able to explain key procedures, understand why controls are necessary, know what to do when a limit is exceeded, and consistently apply what they have learned on the plant floor.
Recurring audit findings may indicate that corrective actions are addressing symptoms rather than root causes. Issues with procedures, training, staffing, accountability, or process design can cause the same problems to return.
Manufacturers can start by assessing patterns across sanitation, training, documentation, environmental monitoring, corrective actions, audits, and plant-level execution. Identifying root causes can help determine which improvements should be prioritized.
An assessment may be beneficial when a manufacturer experiences repeated audit findings, inconsistent practices across shifts or facilities, documentation gaps, recurring microbial findings, or difficulty closing corrective actions.