FDA Inspection 759799 — Physitemp Instruments, LLC

Physitemp Instruments, LLC — FEI 2242483

The FDA completed an inspection of Physitemp Instruments, LLC on Dec 27, 2011 in Clifton, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 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

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