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FDA Inspection 1027110 — Physitemp Instruments, LLC

Physitemp Instruments, LLC — FEI 2242483

The FDA completed an inspection of Physitemp Instruments, LLC on May 4, 2017 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 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Clifton, NJ (United States)

Facility

Other inspections at this facility

  • 1273102 (OAI Wed Jun 18 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1175808 (NAI Wed May 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 759799 (VAI Tue Dec 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources