FDA inspection
Unither Manufacturing LLC.: FDA inspection ending Nov 23, 2010
FDA inspection 703101 · Voluntary Action Indicated (VAI) · Rochester, NY
Key facts
| Inspection ID | 703101 |
|---|---|
| Firm | Unither Manufacturing LLC. |
| FEI number | 1314625 |
| Address | 755 Jefferson Rd |
| City | Rochester |
| State | NY |
| ZIP | 14623 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Nov 23, 2010 |
| 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
- 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