One firm, every FDA signal in one place

A cross‑source lookup: device registrations (openFDA, FEI‑authoritative), recalls, warning letters, and inspection outcomes. Inspections are matched on the firm’s FDA Establishment Identifiers (FEI) where it holds device registrations (verified, same legal site) and by name otherwise — the name path is what surfaces drug and combination‑product firms. Recalls and warning letters are name‑matched, so they can include namesakes or miss differently‑named subsidiaries — verify identity against the owner/operator grouping first.