Home / Inspections / 960553

FDA Inspection 960553 — Laborie Medical Technologies Corp

Laborie Medical Technologies Corp — FEI 3017448360

The FDA completed an inspection of Laborie Medical Technologies Corp on February 22, 2016 in Portsmouth, NH. 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
February 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Portsmouth, NH (United States)

Facility

Other inspections at this facility

  • 1120873 (NAI Wed Feb 26 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 866777 (NAI Thu Feb 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 774570 (NAI Fri Feb 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources