FDA Inspection 859711 — Alma Lasers, Inc.

Alma Lasers, Inc. — FEI 3004450661

The FDA completed an inspection of Alma Lasers, Inc. on December 11, 2013 in Buffalo Grove, IL. 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
December 11, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Buffalo Grove, IL (United States)