FDA Intel: FDA inspection intelligence for AI and the web

Hey Product Hunt,

I built FDA Intel because FDA inspection records are public but hard to use. Form 483s, warning letters, investigator patterns, import alerts and recalls live in scattered PDFs and tables, and quality teams, CDMOs, consultants and investors still spend days stitching them together before an audit or a diligence call.

FDA Intel organizes that record around your question: a site's inspection history, what an investigator cites most, which 21 CFR sections show up, and the linked source documents.

You can use it in the web app, or connect it in the AI you already use. Add fdaintel.ai/mcp as a custom connector in Claude, ChatGPT or Grok, or in your own personal AI agent or any MCP client, sign in once with OAuth, and ask in plain language. Access is read-only, and answers come back with links to the documents.

Plans and document pricing are at fdaintel.ai/pricing. FDA Intel is independent of the U.S. FDA and provides information only, not legal or regulatory advice.

I would love feedback from anyone in quality, regulatory, supplier diligence or investing in FDA-regulated companies. What would you ask it first?

Yehuda