FDA Inspection 708218 — Kenneth Roggen Associates

Kenneth Roggen Associates — FEI 3003929844

The FDA completed an inspection of Kenneth Roggen Associates on Feb 4, 2011 in Trumbull, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 4, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Trumbull, CT (United States)