FDA Inspection 1192349 — LightScalpel, Inc.
The FDA completed an inspection of LightScalpel, Inc. on Dec 2, 2022 in Bothell, WA. 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
- Dec 2, 2022
- Fiscal Year
- 2023
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Bothell, WA (United States)