FDA Inspection 719340 — Cellu Tissue Corporation

Cellu Tissue Corporation — FEI 3000178036

The FDA completed an inspection of Cellu Tissue Corporation on Apr 7, 2011 in East Hartford, 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 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
East Hartford, CT (United States)