FDA Warning Letter — Mibo Medical Group

Case 558900 — FEI 3011407851

The FDA took a Warning Letter action against Mibo Medical Group on November 20, 2018 (Dallas, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Mibo Medical Group
Date
November 20, 2018
Fiscal Year
2019
Product Type
Devices
Center
CDRH
Location
Dallas, TX (United States)