FDA Device Establishments · JSON-LD · Markdown

MIE AMERICA, INC.

FEI 3000210013 · Complaint File Establishment per 21 CFR 820.198 · Status: Active

FEI Number3000210013
Owner / OperatorMIE GMBH (#9028781)
Address420 BENNETT RD., ELK GROVE VILLAGE, IL, US
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)KPS, IYX
Regulation § (21 CFR)892.1200, 892.1100
Proprietary namesMIE - ORBITER SCINTRON; MIE - SD-X 37 SCINTRON; MIE - DIACAM SCINTRON; MIE - LFOV SCINTRON

External sources

Source: openFDA. Public-domain (CC0).