FDA Warning Letter Explorer

Last checked: Oct 1, 2026 at 19:34 UTC. Latest FDA posting included: Sep 29, 2026.

FDA Warning Letter Explorer: analysis

1,654 letters in the saved dataset.

The published record at a glance

1,654 letters to drug, device and biologics makers since 2021. These counts cover the full dataset; interactive filters apply after the charts load.

Product type
Product typeLetters
Drugs1,312
Medical Devices259
Biologics83
Year issued
Year issuedLetters
2021262
2022230
2023234
2024246
2025406
2026276
Most cited sections and clauses in extracted findings
Most cited sections and clauses in extracted findingsLetters
21 CFR 211.84246
21 CFR 211.100203
21 CFR 211.165164
21 CFR 211.192152
21 CFR 211.22125

Latest from FDA

Browse letters →

Summary

The whole record at a glance. Set a filter on the left and your slice draws over it, then pick a tab to go deeper.

Letters per month

Warning letters issued per month to drug, device and biologics makers, Jan 2021 to Sep 2026. Peak: 96 in Sep 2025. Dashed line: 12-month average, now 32.0 a month. Full months only. Hover the chart for any month.

Top 3 trends

Sections and clauses with the largest comparable count changes.

Top 5 citations

The CFR sections and ISO clauses cited in the most letters. Click one to filter.

Top 5 issue types

What went wrong, as read from the findings. Click one to filter.

Quality terms in the letters

The bigger the word, the more letters in your filter use it. Click words to filter; picking several finds letters that mention all of them.

What the agency keeps finding

Citations are pulled from the letter text. When a filter is on, the dim bar behind each value is the unfiltered total.

Trends

Letters citing each CFR section or ISO clause in a stated finding, by year. Change compares two periods of your choosing; both counts are shown in every row. Click a row to filter.

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Most cited sections and clauses

Letters citing each section. Click a bar to filter; "Details" opens the regulation and its letters.

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The findings, in FDA's own words

The most common violation statement for each section, with how many letters state it. Click a statement to read it in full; click the section number to filter.

What went wrong, by issue type

Model-assisted issue types group the letters by quality topic. Supporting FDA passages appear in letter details where available. A letter counts once per type. Click a bar to filter.

Go deeper

The same filter from more angles.

Method

This snapshot combines FDA index fields, rule-extracted CFR and explicit ISO 13485 citations and findings, and model-assisted issue types, requests and prose findings. Exact ISO clauses and CFR sections remain separate. The versioned device-topic map groups related citations for navigation and comparison; it is editorial grouping, not regulatory equivalence. Top-level descriptions use source excerpts checked against the archived FDA letter, not unchecked AI summaries. These selected passages do not summarize the entire letter. Finding interpretations and categories still require source review. Response timing appears only when supported by verified response wording; a published close-out status does not establish a firm's current compliance.

Scope

Coverage is limited to the letters retained in this saved snapshot. Missing letters or close-out records should not be interpreted as a firm's current regulatory status.

FDA Warning Letter Alerts

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