FDA Device Establishments · JSON-LD · Markdown

KOBAYASHI AMERICA MANUFACTURING, LLC

FEI 3003079019 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active

FEI Number3003079019
Owner / OperatorKOBAYASHI AMERICA MANUFACTURING, LLC (#10049550)
Address245 KRAFT DR, Dalton, GA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)IME
Regulation § (21 CFR)890.5700

External sources

Source: openFDA. Public-domain (CC0).