FDA Device Establishments · JSON-LD · Markdown

TEKNIMED SAS

FEI 3003854593 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3003854593
Owner / OperatorTeknimed (#9040657)
Address11_12 rue d Apollo, L Union Haute-Garonne, 31240, FR
Mandatory US AgentRegulatory/Quality Management Information Source, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NDN
Regulation § (21 CFR)888.3027

External sources

Source: openFDA. Public-domain (CC0).