FDA inspection
Monobind, Inc.: FDA inspection ending Aug 17, 2005
FDA inspection 390813 · Voluntary Action Indicated (VAI) · Lake Forest, CA
Key facts
| Inspection ID | 390813 |
|---|---|
| Firm | Monobind, Inc. |
| FEI number | 2020726 |
| Address | 100 N Pointe Dr |
| City | Lake Forest |
| State | CA |
| ZIP | 92630-2270 |
| Fiscal year | 2005 |
| Inspection end date | Aug 17, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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