FDA inspection
Implant Direct Sybron Manufacturing LLC: FDA inspection ending Feb 9, 2005
FDA inspection 394009 · Westlake Village, CA
Key facts
| Inspection ID | 394009 |
|---|---|
| Firm | Implant Direct Sybron Manufacturing LLC |
| FEI number | 3001617766 |
| Address | 3050 E Hillcrest Dr |
| City | Westlake Village |
| State | CA |
| ZIP | 91362-3171 |
| Fiscal year | 2005 |
| Inspection end date | Feb 9, 2005 |
| 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
- 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