FDA inspection
Grand River Aseptic Manufacturing, Inc.: FDA inspection ending Feb 22, 2013
FDA inspection 819903 · Official Action Indicated (OAI) · Grand Rapids, MI
Key facts
| Inspection ID | 819903 |
|---|---|
| Firm | Grand River Aseptic Manufacturing, Inc. |
| FEI number | 3008716173 |
| Address | 140 Front Ave Sw Ste 3 |
| City | Grand Rapids |
| State | MI |
| ZIP | 49504-6426 |
| Fiscal year | 2013 |
| Inspection end date | Feb 22, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | New Drug Evaluation |
| 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