FDA Warning Letter — Biomedix Wai

Case 598171 — FEI 1000115518

The FDA took a Warning Letter action against Biomedix Wai on February 12, 2020 (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
February 12, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Chanhassen, MN (United States)