FDA Inspection 1175808 — Physitemp Instruments, LLC

Physitemp Instruments, LLC — FEI 2242483

The FDA completed an inspection of Physitemp Instruments, LLC on May 25, 2022 in Clifton, 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
May 25, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Clifton, NJ (United States)