# FUJIFILM Diosynth Biotechnologies Denmark ApS, Hillerod, Denmark – FDA Inspections

Source: https://www.keypedia.com/companies/fujifilm-diosynth-biotechnologies-denmark-aps/513b3c42-1517-43bc-936a-d3edd26bed70

> Inspection records and compliance data for FUJIFILM Diosynth Biotechnologies Denmark ApS in Hillerod. 10 FDA inspections on record, 4 Form 483s, last inspected November 12, 2024.

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## Details

- Name: FUJIFILM Diosynth Biotechnologies Denmark ApS
- FEI Number: 3006339887
- Address Line 1: Biogen Idec Alle 1
- City: Hillerod
- Country Name: Denmark
- Address: Biogen Idec Alle 1, Hillerod, Denmark
- Country: Denmark

## Related Documents

- [483 - FUJIFILM Diosynth Biotechnologies Denmark ApS - Unknown Date](https://www.keypedia.com/records/483/fujifilm-diosynth-biotechnologies-denmark-aps/dacf2be1-401f-42e7-be9f-581ec8fa0c39) — source: FDA, date: Invalid Date
- [483 - FUJIFILM Diosynth Biotechnologies Denmark ApS - Unknown Date](https://www.keypedia.com/records/483/fujifilm-diosynth-biotechnologies-denmark-aps/c200d7db-84cd-42a6-91b1-21de41d8d2ac) — source: FDA, date: Invalid Date
- [483 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2024-11-12](https://www.keypedia.com/records/483/fujifilm-diosynth-biotechnologies-denmark-aps/2ec35f9a-5f16-4fee-ad57-6599d261113d) — source: FDA, date: November 12, 2024
- [FDA Inspection 1257821 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2024-11-12](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/2e61f960-1dde-4dbe-83d0-3ed888339059) — source: FDA, date: November 12, 2024
- FDA Inspection 1230111 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2023-06-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 30, 2023
- FDA Inspection 1123030 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2019-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2019
- [FDA Inspection 1084340 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2019-02-12](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/3b6bda6e-28b6-4236-a023-7a0258ac1a76) — source: FDA, date: February 12, 2019
- [FDA Inspection 1052912 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2018-04-13](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/5d0b36e8-6a9e-40ed-a1f0-176156dc7bc2) — source: FDA, date: April 13, 2018
- [FDA Inspection 1030927 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2017-10-31](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/2918676d-486e-4fa0-9a60-9151bf9f52b4) — source: FDA, date: October 31, 2017
- FDA Inspection 1030379 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2017-06-16 — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2017
- FDA Inspection 893674 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2014-08-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 19, 2014
- FDA Inspection 761546 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2011-12-02 — classification: No Action Indicated (NAI), source: FDA, date: December 2, 2011
- [FDA Inspection 737746 - FUJIFILM Diosynth Biotechnologies Denmark ApS - 2011-05-27](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/5d6fe364-ad2f-4c8f-b933-0d12bd322f17) — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2011

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