FDA Inspection 977037 — Motion Lab Systems Inc

Motion Lab Systems Inc — FEI 3001606886

The FDA completed an inspection of Motion Lab Systems Inc on Jul 12, 2016 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
Jul 12, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Baton Rouge, LA (United States)