The U.S. Food and Drug Administration’s Minneapolis District Office sent just a single device-related warning letter in 2010 after more than 140 inspections in Minnesota, Wisconsin and the Dakotas.
The FDA shared the news Wednesday at an annual breakfast with local FDA leaders, sponsored by LifeScience Alley. It was the first opportunity for some to hear from Minneapolis District Director Gerald Berg, a St. Paul native who assumed leadership of the local office in August.