Minnesota State Wire

In May, three Devices companies received three FDA inspections in Minnesota, according to the U.S. Food and Drug Administration (FDA).

This was the highest number of inspections per type of company made by the FDA in Minnesota, equalling 75% of all inspections in May.

Of all the Minnesota companies involved in Devices, LISI MEDICAL Remmele, Inc. received the most citations from the FDA in May.

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	—
Monitoring of Marketed Animal Drugs, Feed, and Devices	1	—	—