FDA inspection
Composite Manufacturing, Inc: FDA inspection ending Jul 18, 2008
FDA inspection 542202 · Voluntary Action Indicated (VAI) · San Clemente, CA
Key facts
| Inspection ID | 542202 |
|---|---|
| Firm | Composite Manufacturing, Inc |
| FEI number | 1000519805 |
| Address | 970 Calle Amanecer Ste B |
| City | San Clemente |
| State | CA |
| ZIP | 92673-6250 |
| Fiscal year | 2008 |
| Inspection end date | Jul 18, 2008 |
| 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