FDA inspection
Ben Venue Laboratories Inc: FDA inspection ending May 25, 2011
FDA inspection 729039 · Official Action Indicated (OAI) · Bedford, OH
Key facts
| Inspection ID | 729039 |
|---|---|
| Firm | Ben Venue Laboratories Inc |
| FEI number | 1519257 |
| Address | 300 Northfield Rd |
| City | Bedford |
| State | OH |
| ZIP | 44146 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | May 25, 2011 |
| Classification | Official Action Indicated (OAI) |
| 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