FDA inspection
Arcet Equipment Company: FDA inspection ending May 18, 2010
FDA inspection 662056 · Voluntary Action Indicated (VAI) · Chester, VA
Key facts
| Inspection ID | 662056 |
|---|---|
| Firm | Arcet Equipment Company |
| FEI number | 1000123092 |
| Address | 13320 Ramblewood Dr |
| City | Chester |
| State | VA |
| ZIP | 23836 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | May 18, 2010 |
| 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