FDA Inspection 1240553 — UltraSPECT USA LLC

UltraSPECT USA LLC — FEI 3018788582

The FDA completed an inspection of UltraSPECT USA LLC on May 7, 2024 in Johnson City, 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
May 7, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Johnson City, TN (United States)