FDA inspection
Mobius Therapeutics LLC: FDA inspection ending Jan 17, 2013
FDA inspection 813405 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 813405 |
|---|---|
| Firm | Mobius Therapeutics LLC |
| FEI number | 3008725026 |
| Address | 4041 Forest Park Ave |
| City | Saint Louis |
| State | MO |
| ZIP | 63108 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Jan 17, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 1–9 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