FDA inspection
GC Hanford Manufacturing Company: FDA inspection ending Nov 30, 2012
FDA inspection 808118 · Voluntary Action Indicated (VAI) · Syracuse, NY
Key facts
| Inspection ID | 808118 |
|---|---|
| Firm | GC Hanford Manufacturing Company |
| FEI number | 1310197 |
| Address | 304 Oneida St |
| City | Syracuse |
| State | NY |
| ZIP | 13202 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 30, 2012 |
| 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