FDA Inspection 1048581 — Curae'Lase, Inc.
The FDA completed an inspection of Curae'Lase, Inc. on February 5, 2018 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
- February 5, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Loris, SC (United States)