FDA Inspection 562346 — Implant Direct Sybron Manufacturing LLC
The FDA completed an inspection of Implant Direct Sybron Manufacturing LLC on Jan 27, 2009 in Westlake Village, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jan 27, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Westlake Village, CA (United States)