FDA Device Establishments · JSON-LD · Markdown

Akesis Inc.

FEI 3015621321 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3015621321
Owner / OperatorAkesis Inc (#10088577)
Address5129 Commercial Circle, Concord, CA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)IWB
Regulation § (21 CFR)892.5750
Proprietary namesGalaxy RTi

External sources

Source: openFDA. Public-domain (CC0).