FDA Inspection 547811 — R. Lewis Inc

R. Lewis Inc — FEI 1000112499

The FDA completed an inspection of R. Lewis Inc on Nov 13, 2008 in Metairie, 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
Nov 13, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Metairie, LA (United States)