FDA Inspection 1312658 — AUDICUS

AUDICUS — FEI 3035551790

The FDA completed an inspection of AUDICUS on Apr 9, 2026 in New York, NY. 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 9, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
New York, NY (United States)

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