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FDA Inspection 991423 — FUJIFILM Healthcare Americas Corporation

FUJIFILM Healthcare Americas Corporation — FEI 1000513161

The FDA completed an inspection of FUJIFILM Healthcare Americas Corporation on October 31, 2016 in Lexington, MA. 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
October 31, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Lexington, MA (United States)

Facility

Other inspections at this facility

  • 1095860 (VAI Fri Jun 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1046796 (VAI Thu Mar 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 994698 (NAI Thu Nov 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919044 (VAI Thu Feb 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 810738 (VAI Wed Dec 12 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources