# FUJIFILM Diosynth Biotechnologies UK Limited – FDA Inspection, Mar 17, 2023

Source: https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-uk-limited/4d6a78ce-42f0-4143-ab86-759495398523
Source feed: FDA_Inspections

> FDA inspection 1200417 of FUJIFILM Diosynth Biotechnologies UK Limited, March 17, 2023. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1200417
- Company Name: FUJIFILM Diosynth Biotechnologies UK Limited
- Inspection Date: 2023-03-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- [FDA Inspection 1339338 - 2026-09-01](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-uk-limited/0a62dc79-bae4-40e3-85e2-01849cc7cb02)
- FDA Inspection 1155694 - 2021-03-25
- FDA Inspection 1097949 - 2018-11-16
- [FDA Inspection 894612 - 2014-07-11](https://www.keypedia.com/records/fda_inspections/fujifilm-diosynth-biotechnologies-uk-limited/ac5f17ff-d054-4ba5-9a1a-a21b8ebc2b8c)
- FDA Inspection 790405 - 2012-06-20

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/libia-m-lugo/893802aa-76a6-4fb5-ab71-eaee099e4f67)

Company: https://www.keypedia.com/companies/fujifilm-diosynth-biotechnologies-uk-limited/1ab271fe-bbf2-4dec-a2b8-1ae59ca0f082

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