FDA inspection
Grand River Aseptic Manufacturing, Inc.: FDA inspection ending Aug 28, 2013
FDA inspection 846300 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 846300 |
|---|---|
| Firm | Grand River Aseptic Manufacturing, Inc. |
| FEI number | 3008716173 |
| Address | 140 Front Ave Sw Ste 3 |
| City | Grand Rapids |
| State | MI |
| ZIP | 49504 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Aug 28, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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