FDA Device Establishments · JSON-LD · Markdown

KWIK TEK, INC.

FEI 3000159466 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3000159466
Owner / OperatorAQUA LEISURE RECREATION LLC (#1221480)
Address12000 E 45th Ave, Denver, CO, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)HOY
Regulation § (21 CFR)886.4750
Proprietary namesDOLFINO GOGGLE

External sources

Source: openFDA. Public-domain (CC0).