Compliance Dashboards

Explore and analyze public FDA data within the below compliance-related datasets.

Inspections icon


U.S. domestic and foreign inspections by fiscal year, classification, product type, etc.

Compliance Actions icon

Compliance Actions

Warning letters, injunctions and seizures by fiscal year, product type, etc.

Recalls icon


Recalls by fiscal year, classification, product type, status, etc.

Imports Summary icon

Imports Summary

Imports summary data by fiscal year, import lines, product categories, countries, etc.

Import Refusals icon

Import Refusals

Import refusals by fiscal year, product categories, country, divisions, etc.

About the Data

The underlying data used to generate the dashboard graphs are based upon transparency datasets and other data already available to the public through the website. The datasets and data include the Inspection Database, and selected data elements from the compliance and enforcement related information on Additional data will be included in future releases of the Dashboard. You may find the location and additional information about each dataset and other data sources by clicking on the links below:

Recall data used in this Dashboard are based upon the Enforcement Reports. For more detailed information about individual recalls, please see the Enforcement Reports and Recalls, Market Withdrawals & Safety Alerts webpages.

Inspectional and compliance data are refreshed on a monthly basis and only include final actions.

Please note that each individual dashboard page provides information pertaining to the data provided. These caveats provide guidance on the data being reported, data limitations and information on what the data represents. Additionally the following information is provided in an effort to enhance the user experience and define data limitations. All underlying data used to create the graphical representations are pulled from FDA’s transactional systems and are subject to change.

  1. Not all inspections are included in the database. Inspections conducted by States, pre-approval inspections, inspections waiting for a final enforcement action, and inspections of nonclinical labs are not included. Inspections of nonclinical labs are available at Nonclinical Laboratories Inspected under Good Laboratory Practices.
  2. The results show final classifications of No Action Indicated (NAI), Voluntary Action Indicated (VAI), Official Action Indicated (OAI) for each project area within an inspection.
  3. Compliance data provide information on a subset of the actions used by the FDA to bring firms into compliance, specifically data pertaining to Warning Letters, Seizures, and Injunctions. The compliance actions disclosed include only finalized and completed actions and are primarily used in the domestic arena. Actions pertaining to foreign firms often take the form of import alerts.