FDA 483 OBSERVATION · #461 OF 1,000 MOST-CITED
Equipment - automated - calibrate, inspect
FDA cited this observation 41 times across 35 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 3.1× the rate of the average FDA-cited firm (25.7% vs 8.3%), across 35 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
You did not routinely calibrate the automated, mechanical, or electronic equipment to ensure proper performance.
You did not routinely calibrate the automated, mechanical, or electronic equipment to ensure proper performance.
You did not routinely calibrate, inspect and check the automated, mechanical, or electronic equipment to ensure proper performance.
You did not routinely calibrate the automated, mechanical, or electronic equipment to ensure proper performance.
You did not routinely inspect and check the automated, mechanical, or electronic equipment to ensure proper performance.
You did not routinely calibrate the automated, mechanical, or electronic equipment to ensure proper performance.
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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