FDA inspection
FujiFilm Diosynth Biotechnologies U.S.A., Inc.: FDA inspection ending Mar 27, 2026
FDA inspection 1309990 · Research Triangle Park, NC
Key facts
| Inspection ID | 1309990 |
|---|---|
| Firm | FujiFilm Diosynth Biotechnologies U.S.A., Inc. |
| FEI number | 3000718852 |
| Address | 6051 George Watts Hill Dr |
| City | Research Triangle Park |
| State | NC |
| ZIP | 27709 |
| Fiscal year | 2026 |
| Inspection end date | Mar 27, 2026 |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data