FDA inspection
Arcoma North America, Inc.: FDA inspection ending Sep 11, 2014
FDA inspection 895596 · Voluntary Action Indicated (VAI) · Laguna Hills, CA
Key facts
| Inspection ID | 895596 |
|---|---|
| Firm | Arcoma North America, Inc. |
| FEI number | 3005998708 |
| Address | 23112 Alcalde Dr Ste A |
| City | Laguna Hills |
| State | CA |
| ZIP | 92653 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Sep 11, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
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