FDA Inspection 768936 — Implant Direct Sybron Manufacturing LLC
The FDA completed an inspection of Implant Direct Sybron Manufacturing LLC on Feb 10, 2012 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
- Feb 10, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Westlake Village, CA (United States)