FDA Inspection 759799 — Physitemp Instruments, LLC

Physitemp Instruments, LLC — FEI 2242483

The FDA completed an inspection of Physitemp Instruments, LLC on December 27, 2011 in Clifton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 27, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Clifton, NJ (United States)

Citations

IDCFRDescription
332821 CFR 820.180(b)Retention period