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FDA Inspection 1030379 — FUJIFILM Diosynth Biotechnologies Denmark ApS

FUJIFILM Diosynth Biotechnologies Denmark ApS — FEI 3006339887

The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies Denmark ApS on June 16, 2017 in Hillerod. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
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))
  • 893674 (VAI Tue Aug 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 761546 (NAI Fri Dec 02 2011 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