FDA Warning Letter — Owen Mumford USA, Inc.

Case 423170 — FEI 1000219614

The FDA took a Warning Letter action against Owen Mumford USA, Inc. on June 4, 2014 (Marietta, GA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Owen Mumford USA, Inc.
Date
June 4, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Marietta, GA (United States)