FDA Inspection 1222755 — UltraRad Corporation

UltraRad Corporation — FEI 3000149131

The FDA completed an inspection of UltraRad Corporation on August 18, 2023 in Voorhees, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 18, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Voorhees, NJ (United States)