FDA 483 OBSERVATION · #1264 OF 1,932 MOST-CITED
Adverse Reaction - Investigations
FDA cited this observation 11 times across 10 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 grouping is not
An observation-type page groups FDA’s published citation records. The grouping, the compliance steps and the root causes are SPEQ synthesis, not an FDA classification of any citation, and a count measures what FDA published rather than risk.
How FDA worded it — real examples
A thorough investigation of each reported adverse reaction was not made.
A thorough investigation of each reported adverse reaction was not made.
A thorough investigation of each reported adverse reaction was not made.
A thorough investigation of each reported adverse reaction was not made.
A thorough investigation of each reported adverse reaction was not made.
A thorough investigation of each reported adverse reaction was not made.
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. Open the 483 observation explorer →