FDA Device Establishments · JSON-LD · Markdown

KITRON AB

FEI 3009834076 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3009834076
Owner / OperatorKitron AB (#10042519)
AddressMobelvagen 5, Jonkoping, SE-55652, SE
Mandatory US AgentFDA Agent Pro LLC
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)JOY
Regulation § (21 CFR)864.5260
Proprietary namesCellaVision DC-1

External sources

Source: openFDA. Public-domain (CC0).