FDA Inspection 675278 — Syneron, Inc.
The FDA completed an inspection of Syneron, Inc. on Aug 6, 2010 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Aug 6, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Irvine, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 3125 | 21 CFR 820.80(d) | Lack of or inadequate final acceptance procedures |
| 3168 | 21 CFR 820.198(a) | Complaints |
| 3375 | 21 CFR 820.198(e) | Records of complaint investigation |