FDA Warning Letter — Sterilmed Inc.

Case 228956 — FEI 3001237663

The FDA took a Warning Letter action against Sterilmed Inc. on Oct 26, 2011 (Maple Grove, MN). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Sterilmed Inc.
Date
Oct 26, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Maple Grove, MN (United States)