FDA Device Establishments · JSON-LD · Markdown

AMPLITUDE

FEI 3009590742 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3009590742
Owner / OperatorAMPLITUDE (#10054515)
Address11 Cours Jacques Offenbach, Zone Mozart 2, Valence Drome, 26000, FR
Mandatory US AgentFDAbasics
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)JWH
Regulation § (21 CFR)888.3560

External sources

Source: openFDA. Public-domain (CC0).