FDA Warning Letter — H & A Mui Enterprises, Inc.

Case 227795 — FEI 3002807135

The FDA took a Warning Letter action against H & A Mui Enterprises, Inc. on November 22, 2011 (Mississauga, Canada). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
H & A Mui Enterprises, Inc.
Date
November 22, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Mississauga (Canada)