FDA Inspection 1278866 — ULTRAVISION CORPORATION

ULTRAVISION CORPORATION — FEI 3008223664

The FDA completed an inspection of ULTRAVISION CORPORATION on Jul 25, 2025 in North Palm Beach, FL. 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
Jul 25, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
North Palm Beach, FL (United States)

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