FDA Inspection 1313768 — Zinnovi Inc

Zinnovi Inc — FEI 3031823608

The FDA completed an inspection of Zinnovi Inc on Apr 16, 2026 in Schaumburg, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 16, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Schaumburg, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.