FDA Warning Letter — Interojo Inc.

Case 381558 — FEI 3004146030

The FDA took a Warning Letter action against Interojo Inc. on January 7, 2013 (Pyeongtaek City, South Korea). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Interojo Inc.
Date
January 7, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Pyeongtaek City (South Korea)