In November 2024, four Devices companies received four FDA inspections in Minnesota, according to the U.S. Food and Drug Administration (FDA).
This was the second highest number of inspections per type of company made by the FDA in Minnesota, equalling 19% of all inspections in November 2024.
Of all the Minnesota companies involved in Devices, Pathy Medical, LLC received the most citations from the FDA in November 2024.
The FDA routinely inspects facilities across the nation to determine if the workplace and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly.
According to its website, the FDA is a government agency that is primarily responsible for monitoring the production and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety quality.
| Project Area | No Action Indicated | Voluntary Action Indicated | Official Action Indicated |
|---|---|---|---|
| Blood and Blood Products | 1 | — | — |
| Compliance: Devices | 3 | 1 | — |
| Drug Quality Assurance | 1 | — | — |
| Foodborne Biological Hazards | 4 | 5 | — |
| Monitoring of Marketed Animal Drugs, Feed, and Devices | — | 1 | — |
| Postmarket Assurance: Devices | 3 | — | — |
| Technical Assistance: Food and Cosmetics | 5 | — | — |
