FDA Inspection 1256347 — I/O Urology Corporation

I/O Urology Corporation — FEI 3030244515

The FDA completed an inspection of I/O Urology Corporation on Oct 30, 2024 in Knoxville, TN. 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
Oct 30, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Knoxville, TN (United States)

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