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FDA Inspection 761546 — FUJIFILM Diosynth Biotechnologies Denmark ApS

FUJIFILM Diosynth Biotechnologies Denmark ApS — FEI 3006339887

The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies Denmark ApS on December 2, 2011 in Hillerod. 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
December 2, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Hillerod (Denmark)

Facility

Other inspections at this facility

  • 1230111 (VAI Fri Jun 30 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1123030 (VAI Fri May 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1030379 (NAI Fri Jun 16 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 893674 (VAI Tue Aug 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737746 (NAI Fri May 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources