FDA Device Establishments · JSON-LD · Markdown

GERMITEC

FEI 3030303856 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3030303856
Owner / OperatorGERMITEC (#10091485)
Address19 rue Vauban, Bordeaux Nouvelle-Aquitaine, 33000, FR
Mandatory US AgentGermitec
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)SCS
Regulation § (21 CFR)880.6511
Proprietary namesCHRONOS

External sources

Source: openFDA. Public-domain (CC0).