FDA Inspection 638610 — Motion Lab Systems Inc

Motion Lab Systems Inc — FEI 3001606886

The FDA completed an inspection of Motion Lab Systems Inc on Jan 14, 2010 in Baton Rouge, LA. 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
Jan 14, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Baton Rouge, LA (United States)