FDA 483 OBSERVATION · #445 OF 1,000 MOST-CITED
HACCP plan - corrective action plan not included
FDA cited this observation 55 times across 49 firms in recent inspections. Below: how it breaks down by program area and fiscal year, and real examples of how FDA worded it on Form FDA 483.
What this observation is associated with
Firms cited for this observation also appear in FDA compliance actions — warning letters, injunctions, or seizures — at 1.3× the rate of the average FDA-cited firm (10.2% vs 7.7%), across 49 FEI-matched firms.
This is an association, not causation, and reflects co-occurrence in FDA's records — not a claim that the observation caused or preceded the action.
How FDA worded it — real examples
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure the cause of the deviation was corrected.
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure affected product is not entered into commerce and the cause of the deviation was corrected.
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure.
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure affected product is not entered into commerce.
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure the cause of the deviation was corrected.
Your HACCP plan includes a corrective action plan that is not in accordance with 21 CFR 120.10(a) to ensure the cause of the deviation was corrected.
Related SPEQ references
Where to read the requirements behind this observation area on SPEQ. These are SPEQ's topic and audience pages — not an FDA classification of the citation.
Examples are a representative sample of FDA's published inspection observations. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.
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