FDA inspection
Implant Direct Sybron Manufacturing LLC: FDA inspection ending Jan 27, 2009
FDA inspection 562346 · No Action Indicated (NAI) · Westlake Village, CA
Key facts
| Inspection ID | 562346 |
|---|---|
| Firm | Implant Direct Sybron Manufacturing LLC |
| FEI number | 3001617766 |
| Address | 3050 E Hillcrest Dr |
| City | Westlake Village |
| State | CA |
| ZIP | 91362 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jan 27, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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