FDA 483 OBSERVATION · #541 OF 1,000 MOST-CITED
Acceptance of drug products
FDA cited this observation 45 times across 44 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 4.1× the rate of the average FDA-cited firm (31.8% vs 7.7%), across 44 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
Determinations of conformance to appropriate written specifications for acceptance are deficient for drug products.
Determinations of conformance to appropriate written specifications for acceptance are deficient for drug products.
Determinations of conformance to appropriate written specifications for acceptance are deficient for drug products.
Determinations of conformance to appropriate written specifications for acceptance are not made and deficient for drug products. Electronic records are used, but they do not meet requirements to ensure that they are trustworthy, reliable and generally equivalent to paper records.
Determinations of conformance to appropriate written specifications for acceptance are not made for drug products.
Determinations of conformance to appropriate written specifications for acceptance are not made for drug products.
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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