FDA Inspection 635950 — Eversight

Eversight — FEI 3002291793

The FDA completed an inspection of Eversight on Dec 15, 2009 in Middletown, 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
Dec 15, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Middletown, CT (United States)