FDA Warning Letter — ARB Medical, LLC

Case 482215 — FEI 3005770977

The FDA took a Warning Letter action against ARB Medical, LLC on December 22, 2015 (Minnetonka, MN). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
ARB Medical, LLC
Date
December 22, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Minnetonka, MN (United States)