FDA Device Establishments · JSON-LD · Markdown

AKERVALL TECHNOLOGIES

FEI 3011547262 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility · Status: Active

FEI Number3011547262
Owner / OperatorAkervall Technologies Inc. (#10048970)
Address1512 Woodland Dr, Saline, MI, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)EFT
Regulation § (21 CFR)872.3520

External sources

Source: openFDA. Public-domain (CC0).