The FDA conducted a total of three inspections at three different medical device firms in North Dakota during 2025, according to the U.S. Food and Drug Administration (FDA).
This number represented the second lowest count of inspections per company type carried out by the FDA in North Dakota, accounting for 4.1% of all inspections conducted that year.
Among all medical device companies in North Dakota, Michael D. Greenwood, M.D. received the highest number of citations from the FDA in 2025.
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 and quality.
| Project Area | No Action Indicated | Voluntary Action Indicated | Official Action Indicated |
|---|---|---|---|
| Bioresearch Monitoring | — | 1 | — |
| Blood and Blood Products | 2 | 5 | — |
| Compliance: Devices | 2 | — | — |
| Food Composition, Standards, Labeling and Econ | 7 | 2 | — |
| Foodborne Biological Hazards | 35 | 4 | — |
| Human Cellular, Tissue, and Gene Therapies | 2 | — | — |
| Monitoring of Marketed Animal Drugs, Feed, and Devices | — | 1 | — |
| Postmarket Assurance: Devices | 2 | — | — |
| Technical Assistance: Food and Cosmetics | 21 | — | — |
