FDA Inspection 557929 — Ivoclar Vivadent Manufacturing, Inc.
The FDA completed an inspection of Ivoclar Vivadent Manufacturing, Inc. on Jan 21, 2009 in Somerset, NJ. 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 21, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Somerset, NJ (United States)