FDA Inspection 871148 — Eversight

Eversight — FEI 3002291793

The FDA completed an inspection of Eversight on Mar 21, 2014 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
Mar 21, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Middletown, CT (United States)