FDA Inspection 1326480 — Physitemp Instruments, LLC

Physitemp Instruments, LLC — FEI 2242483

The FDA completed an inspection of Physitemp Instruments, LLC on Jul 10, 2026 in Clifton, NJ. 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 10, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Clifton, NJ (United States)

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