FDA Inspection 810308 — Laser Wellness, Inc.

Laser Wellness, Inc. — FEI 3007682546

The FDA completed an inspection of Laser Wellness, Inc. on December 6, 2012 in Rapid City, SD. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 6, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Rapid City, SD (United States)