FDA Device Establishments · JSON-LD · Markdown

INTEROJO INC.

FEI 3004146030 · Manufacture Medical Device · Status: Active

FEI Number3004146030
Owner / OperatorINTEROJO INC. (#9058386)
Address28& 25 Sandan-ro 15 beon-gil, PYONGTAEK-CITY Gyeonggi, --, KR
Mandatory US AgentEYEREG CONSULTING, INC.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LPL
Regulation § (21 CFR)886.5925
Proprietary namesPV; HD; HDT; PVT

External sources

Source: openFDA. Public-domain (CC0).