Minnesota State Wire

In June, three Devices companies received three 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 27.3% of all inspections in June.

Of all the Minnesota companies involved in Devices, Medspira, LLC received the most citations from the FDA in June.

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
Compliance: Devices	2	1	—
Foodborne Biological Hazards	4	—	—
Human Cellular, Tissue, and Gene Therapies	1	—	—
Monitoring of Marketed Animal Drugs, Feed, and Devices	2	—	—
Postmarket Assurance: Devices	3	—	—
Technical Assistance: Food and Cosmetics	2	—	—