FDA Inspection Database

Type a company, facility, city, or investigator name into the search box at the top of this page. Atlas returns matching facilities, investigators, and Form 483s as you type, and each result opens with its full inspection history. To browse instead, start from the FDA Form 483 database, the FDA investigator lookup, or the facility lookup.

Search the company here and open its facility page. Each facility page lists every FDA inspection on record with its outcome, the Form 483s it received, the investigators who inspected it, and the regulations it is cited for most. The Excel Vision facility in Annonay, France, for example, links straight to its January 2026 Form 483 and its 13 observations.

Atlas connects records the FDA keeps in separate places. One search links an investigator to every facility they inspected, a facility to every Form 483 it received, and each observation to the regulation it cites. Book a demo to see the verbatim observations, source PDFs, and company responses behind each record.

Continuously. New inspection data typically reaches Atlas within a business week, often before it appears on the FDA website, and the investigator, facility, and Form 483 pages update when it does. For the trend across all of it, the US FDA inspections dashboard charts inspections by year, country, and outcome.

Yes. Alongside FDA inspections, Form 483s, and warning letters, Atlas covers five international agencies: the MHRA in the UK, PMDA in Japan, Health Canada, CDSCO in India, and Swissmedic. It also tracks import alerts, recalls, debarment letters, and complete response letters. The Health Canada inspections report is one example.