FDA Warning Letter — Eaton Manufacturing Corporation Dba Eaton Medical

Case 119929 — FEI 1000113105

The FDA took a Warning Letter action against Eaton Manufacturing Corporation Dba Eaton Medical on July 27, 2010 (Memphis, TN). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Eaton Manufacturing Corporation Dba Eaton Medical
Date
July 27, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Memphis, TN (United States)