FDA inspection
FUJIFILM Diosynth Biotechnologies Denmark ApS: FDA inspection ending Jun 16, 2017
FDA inspection 1030379 · No Action Indicated (NAI) · Hillerod
Key facts
| Inspection ID | 1030379 |
|---|---|
| Firm | FUJIFILM Diosynth Biotechnologies Denmark ApS |
| FEI number | 3006339887 |
| Address | Biogen Idec Alle 1 |
| City | Hillerod |
| Country | Denmark |
| Fiscal year | 2017 |
| Inspection end date | Jun 16, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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