# FDA Inspection 1123030 - FUJIFILM Diosynth Biotechnologies Denmark ApS - May 10, 2019

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-denmark-aps/a4f96127-56da-4dff-a7f0-e7cace980ec4
Source feed: FDA_Inspections

> FDA Inspection 1123030 for FUJIFILM Diosynth Biotechnologies Denmark ApS on May 10, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1123030
- Company Name: FUJIFILM Diosynth Biotechnologies Denmark ApS
- Inspection Date: 2019-05-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

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

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c