FDA Inspection 811634 — Curae'Lase, Inc.
The FDA completed an inspection of Curae'Lase, Inc. on November 6, 2012 in Loris, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 6, 2012
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Loris, SC (United States)