FDA Warning Letter — Biomedix Wai

Case 394520 — FEI 1000115518

The FDA took a Warning Letter action against Biomedix Wai on June 14, 2013 (Chanhassen, MN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Biomedix Wai
Date
June 14, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Chanhassen, MN (United States)