FDA Device Establishments · JSON-LD · Markdown

ARLINGTON SPECIALTIES, INC.

FEI 3011050481 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active

FEI Number3011050481
Owner / OperatorArlington Specialties, Inc. (#10047238)
Address1515 Carmen Drive, Elk Grove Village, IL, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)JES
Regulation § (21 CFR)872.6390
Proprietary namesPinch Provisions

External sources

Source: openFDA. Public-domain (CC0).