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FDA Warning Letter — Interojo Inc.

Case 381558 — FEI 3004146030

The FDA took a Warning Letter action against Interojo Inc. on Jan 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
Jan 7, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Pyeongtaek City (South Korea)

Facility

Recent inspections

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.