FDA Inspection 720841 — Revue International LLC

Revue International LLC — FEI 1219429

The FDA completed an inspection of Revue International LLC on Apr 15, 2011 in Norwalk, CT. 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
Apr 15, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Norwalk, CT (United States)