FDA Inspection 654291 — Lasag Industrial Lasers

Lasag Industrial Lasers — FEI 3005929230

The FDA completed an inspection of Lasag Industrial Lasers on Mar 23, 2010 in Buffalo Grove, IL. 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
Mar 23, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Buffalo Grove, IL (United States)