FDA inspection
FujiFilm Diosynth Biotechnologies U.S.A., Inc.: FDA inspection ending Oct 26, 2018
FDA inspection 1080402 · Research Triangle Park, NC
Key facts
| Inspection ID | 1080402 |
|---|---|
| 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 | 2019 |
| Inspection end date | Oct 26, 2018 |
| Project area | New Drug Evaluation |
| 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