FDA Warning Letter — Med-Mizer, Inc.

Case 423788 — FEI 3004976058

The FDA took a Warning Letter action against Med-Mizer, Inc. on July 22, 2014 (Batesville, IN). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Med-Mizer, Inc.
Date
July 22, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Batesville, IN (United States)