FDA Inspection 778063 — Eversight

Eversight — FEI 3002291793

The FDA completed an inspection of Eversight on Apr 20, 2012 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
Apr 20, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Middletown, CT (United States)