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FDA Inspection 985390 — Nidek Medical Products Inc

Nidek Medical Products Inc — FEI 1039215

The FDA completed an inspection of Nidek Medical Products Inc on August 16, 2016 in Birmingham, AL. 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
August 16, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Birmingham, AL (United States)

Facility

Other inspections at this facility

  • 855858 (NAI Wed Nov 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 775100 (OAI Tue Apr 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 650979 (VAI Wed Feb 24 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources