In March, one Devices company received an FDA inspection in Tennessee, according to the U.S. Food and Drug Administration (FDA).
This was the lowest number of inspections per type of company made by the FDA in Tennessee, equalling 10% of all inspections in March.
The FDA routinely inspects facilities across the nation to determine if the workplaces and their products are compliant with FDA-regulated laws and regulations implemented to improve overall public health. Inspection results are then disclosed publicly for businesses to consistently make smarter business decisions for the future.
The FDA is a government agency primarily responsible for monitoring the manufacturing and distribution of human and animal drugs, biological products, medical supplies and tobacco products for safety quality, according to its website.
| Project Area | No Action Indicated | Voluntary Action Indicated | Official Action Indicated |
|---|---|---|---|
| Blood and Blood Products | 2 | — | — |
| Compliance: Devices | 1 | — | — |
| Food Composition, Standards, Labeling and Econ | 1 | — | — |
| Foodborne Biological Hazards | 3 | 2 | — |
| Human Cellular, Tissue, and Gene Therapies | 2 | — | — |
| Postmarket Assurance: Devices | 1 | — | — |
