The U.S. Food and Drug Administration (FDA) has sent a warning letter to MRI Imaging Specialist in Norcross, GA, for what the agency called continued violations of the Mammography Quality Standards Act (MQSA).
In a follow-up inspection of the facility on February 19, an FDA representative found one level 1 violation and seven level 2 violations, according to the warning letter. In addition, the practice failed to respond to the MQSA facility inspection report.
The follow-up inspection was performed after two previous noncompliant MQSA inspections on July 1, 2014, and June 17, 2015. The FDA gave MRI Imaging Specialist 15 working days to respond to the March 16 letter and provide the specific steps it has taken or will take to correct and prevent the recurrence of the violations named in the letter and similar violations, including projected time frames. MRI Imaging Specialist will also need to provide sample records that demonstrate proper record-keeping procedures, the FDA said.













![A normal mammogram confirmed by three-year radiologic follow-up illustrates reader-marked regions of interest (ROIs) during (A) unaided (round 1) and (B) artificial intelligence (AI)–assisted (round 2) reading. Each colored dot represents an ROI for recall by a human reader. Readers could mark more than one ROI per case, represented by multiple dots of the same color. During AI-assisted reading, the AI system displayed three visible prompts: two with suspicion of malignancy scores of 35% (left mediolateral oblique [L MLO] and craniocaudal [L CC]) and one with a suspicion of malignancy score of 10% (right craniocaudal [R CC]), shown as polygonal overlays. Without AI, six of 10 readers (60%) marked a false-positive ROI. With AI assistance, this fell to two of 10 (20%). R MLO = right mediolateral oblique.](https://img.auntminnie.com/mindful/smg/workspaces/default/uploads/2026/07/2026-07-14-radiology-mammogram-ai-auto-bias.H0bYO8QlWs.jpg?auto=format%2Ccompress&fit=crop&h=112&q=70&w=112)





