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Brought to you by the Council of the Inspectors General on Integrity and Efficiency
Federal Reports
Report Date
Agency Reviewed / Investigated
Report Title
Type
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Department of Commerce
The Department Needs to Strengthen Its Ethics Oversight for USPTO Patent Examiners
For our evaluation of the United States Patent and Trademark Office’s (USPTO’s) and the U.S. Department of Commerce’s (the Department’s) ethics oversight of USPTO patent examiners, our evaluation objective was to determine whether USPTO and the Department effectively administered ethics rules to prevent financial conflicts of interest by USPTO patent examiners. Overall, we found that USPTO and the Department did not effectively administer the Department’s ethics program to protect against potential conflicts of interest by patent examiners. Specifically, we found that I. USPTO and the Department did not ensure examiners filed confidential financial disclosure reports (CFDRs) as required; II. The Department did not identify or resolve potential financial conflicts in CFDRs; and III. USPTO and the Department did not provide specialized training or guidance to examiners on potential ethics conflicts.
The OIG conducted this inspection to assess the stewardship and oversight of funds by the VA Memphis Healthcare System in Tennessee. This inspection assessed financial activities and administrative processes to determine whether appropriate controls and oversight were in place. These included open obligations, purchase card use, inventory and supply management, and pharmacy operations.After analyzing a judgmental sample of 20 open obligations, the team found that 10 obligations totaling approximately $11.5 million were more than 90 days past the end of the performance period, and the team could not verify whether healthcare system staff reviewed these obligations, as required. In another sample, the team found that four obligations had residual funds of $7,200 that should have been deobligated.Using a sample of 40 purchase card transactions, the team estimated that staff may have made noncompliance errors in over 18,500 transactions resulting in approximately $19.8 million in questioned costs.For inventory and supply management, the team found that training issues, inadequate staffing levels, poor oversight, and data validity issues affected the healthcare system’s stock levels. Healthcare system staff also could not provide documentation to show that required physical inventories were completed or that the chief supply chain officer reviewed the list of personnel with access to the inventory system.The team also found that the healthcare system can further improve pharmacy efficiency by adhering to inventory management best practices, such as adding scannable barcodes to shelving, increasing inventory turnover rates for “A” and “C” items in accordance with Pharmacy Benefit Management target rates, and ensuring compliance with the B09 reconciliation process.The OIG made nine recommendations to the healthcare system director to address the issues identified.
Audit of the Justice Management Division’s Information Security Management Program Pursuant to the Federal Information Security Modernization Act of 2014, Fiscal Year 2023
Audit of the Bureau of Alcohol, Tobacco, Firearms, and Explosive’s Information Security Management Program Pursuant to the Federal Information Security Modernization Act of 2014, Fiscal Year 2023
Audit of the Justice Management Division’s Fix National Instant Criminal Background Check System Disposition Reporting System Pursuant to the Federal Information Security Modernization Act of 2014, Fiscal Year 2023
The OIG inspection team sought tounderstand how the U.S. GovernmentPublishing Office (GPO) maintainsindoor air quality (IAQ) at the CentralComplex Buildings in Washington, DC.
Direct Budget Support: USAID Ensured That the Government of Ukraine Adhered to Required Controls, but Did Not Verify the Accuracy of Salary Expenditures