FDA Inspection
FujiFilm Diosynth Biotechnologies U.S.A., Inc.FujiFilm Diosynth Biotechnologies U.S.A., Inc. – FDA Inspection, Mar 1, 2019
Record Details
This FDA Inspection record concerns FujiFilm Diosynth Biotechnologies U.S.A., Inc., with an inspection on March 1, 2019, issued by the Atlanta District Office, covering human drugs.
- Inspection Date
- March 1, 2019
- Product Type
- Human Drugs
View Company Profile
ID · 633acab5-a082-45ba-af3c-6f6c7690e7c0
Inspection Facts
- Inspection number
- 1092044
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of FujiFilm Diosynth Biotechnologies U.S.A., Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| March 27, 2026 | Not classified | Atlanta District Office | |
| February 10, 2023 | Not classified | Atlanta District Office | |
| October 26, 2018 | Not classified | Atlanta District Office | |
| February 9, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 31, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for FujiFilm Diosynth Biotechnologies U.S.A., Inc.
- FDA Inspection 1309990 - 2026-03-27
- FDA Inspection 1218019 - 2023-02-10
- FDA Inspection 1080402 - 2018-10-26
- FDA Inspection 1045267 - 2018-02-09
- FDA Inspection 989406 - 2016-03-31
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