FDA Inspection 810592 — Laser Light Technologies Inc

Laser Light Technologies Inc — FEI 1000218219

The FDA completed an inspection of Laser Light Technologies Inc on Nov 29, 2012 in Hermann, MO. 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
Nov 29, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Hermann, MO (United States)