FDA Inspection 879751 — S.L.P. Inc

S.L.P. Inc — FEI 3006463573

The FDA completed an inspection of S.L.P. Inc on May 15, 2014 in Elgin, 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
May 15, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Elgin, IL (United States)