FDA Inspection 895132 — Syneron, Inc.
The FDA completed an inspection of Syneron, Inc. on Sep 12, 2014 in Irvine, 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
- Sep 12, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Irvine, CA (United States)