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FDA Inspection 994698 — FUJIFILM Healthcare Americas Corporation

FUJIFILM Healthcare Americas Corporation — FEI 1000513161

The FDA completed an inspection of FUJIFILM Healthcare Americas Corporation on November 10, 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
November 10, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lexington, MA (United States)

Additional Details

Sponsor, Contract Research Organization

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))
  • 991423 (NAI Mon Oct 31 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