FDA inspection
Accupack Midwest Inc: FDA inspection ending Aug 12, 2009
FDA inspection 610579 · Voluntary Action Indicated (VAI) · Cincinnati, OH
Key facts
| Inspection ID | 610579 |
|---|---|
| Firm | Accupack Midwest Inc |
| FEI number | 1000122754 |
| Address | 1060 Meta Dr |
| City | Cincinnati |
| State | OH |
| ZIP | 45237 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Aug 12, 2009 |
| 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
- 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