# FujiFilm Diosynth Biotechnologies U.S.A., Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/fujifilm-diosynth-biotechnologies-usa-inc/44b7fa9f-848c-4e30-869e-12ddcfd848f8

> Inspection records and compliance data for FujiFilm Diosynth Biotechnologies U.S.A., Inc. in Morrisville, NC. Access full analysis and detailed observations.

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## Details

- Name: FujiFilm Diosynth Biotechnologies U.S.A., Inc.
- FEI Number: 3000718852
- City: Morrisville
- State: NC
- Country Name: United States
- Address Line 1: 101 J. Morris Commons Lane
- Zip Code: 27560
- Facility Type: Drug Substance Manufacturer

## Related Documents

- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - Unknown Date](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/866350c6-96dd-4459-961a-5276a841f01c) — source: FDA, date: Invalid Date
- [FDA Inspection 1309990 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2026-03-27](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/6a45f213-b711-4a42-b1b1-724099c2a16d) — source: FDA, date: March 27, 2026
- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2023-02-10](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/4195691b-fc0e-45b6-8d70-bbfc800e6672) — source: FDA, date: February 10, 2023
- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2021-04-21](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/17d024ab-ac04-409b-9487-d3cc9484c5d4) — source: FDA, date: April 21, 2021
- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2021-04-21](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/99e9d1f6-1d51-4a94-a747-2179b07036e0) — source: FDA, date: April 21, 2021
- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2019-03-01](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/c726ae27-0006-43fa-8261-f05e9c6173fb) — source: FDA, date: March 1, 2019
- [FDA Inspection 1045267 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2018-02-09](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/956739fc-b00a-4194-b345-00f56129ccf1) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2018
- [FDA Inspection 989406 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2016-03-31](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/8572110c-bf60-48d4-b637-a431e1705259) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2016
- [483 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2015-05-01](https://www.globalkeysolutions.net/records/483/fujifilm-diosynth-biotechnologies-usa-inc/8e95df71-2fd7-4988-af3d-661e9384b967) — source: FDA, date: May 1, 2015
- [FDA Inspection 848000 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2013-09-12](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/70820fec-b5a9-468f-97f1-c5caf7ee385e) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013
- [FDA Inspection 679053 - FujiFilm Diosynth Biotechnologies U.S.A., Inc. - 2010-07-16](https://www.globalkeysolutions.net/records/fda_inspections/fujifilm-diosynth-biotechnologies-usa-inc/ce785a7c-4ddc-4846-999a-3efbae967b1d) — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2010

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