FDA 483 OBSERVATION · #606 OF 1,000 MOST-CITED
Remedial action
FDA cited this observation 30 times across 28 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.
How FDA worded it — real examples
When test/measurement equipment was found to not meet accuracy and precision limits, inadequate action was taken to evaluate whether there was any adverse effect on the device's quality.
When test/measurement equipment was found to not meet accuracy and precision limits, inadequate action was taken to evaluate whether there was any adverse effect on the device's quality.
When test/measurement equipment was found to not meet accuracy and precision limits, no action was taken to evaluate whether there was any adverse effect on the device's quality.
When test/measurement equipment was found to not meet accuracy and precision limits, inadequate action was taken to evaluate whether there was any adverse effect on the device's quality.
When test/measurement equipment was found to not meet accuracy and precision limits, no action was taken to bring the equipment into calibration.
When test/measurement equipment was found to not meet accuracy and precision limits, no action was taken to evaluate whether there was any adverse effect on the device's quality.
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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