FDA Inspection 920084 — Uno Laser Inc.

Uno Laser Inc. — FEI 3010282401

The FDA completed an inspection of Uno Laser Inc. on January 25, 2015 in Brooklyn, NY. 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
January 25, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Brooklyn, NY (United States)