In 2020, the Food and Drug Administration (FDA) was unable to complete more than 1,000 of its drug inspections, putting the quality of drugs sold on the US market at risk, according to a US Government Accountability Office (GAO) testimony report to a House subcommittee yesterday.Concerns over this backlog have been raised by industry stakeholders as the pandemic has continued, and in GAO's testimony to the Subcommittee on Agriculture, Rural Development, FDA, and Related Agencies, it underscores its inspection-related recommendations from January while adding further insights into inspection trends and potential barriers."Over the years since we first examined this issue, FDA has made significant changes to adapt to the globalization of the