FDA Inspection 1025152 — Remote Technologies, Inc.

Remote Technologies, Inc. — FEI 1000120772

The FDA completed an inspection of Remote Technologies, Inc. on September 14, 2017 in Greenwich, CT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Greenwich, CT (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures
323621 CFR 820.72(b)Calibration procedures - content