FDA Inspection 805412 — Eversight

Eversight — FEI 3000718321

The FDA completed an inspection of Eversight on October 30, 2012 in Ann Arbor, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 30, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Ann Arbor, MI (United States)