FDA Inspection 1028802 — Eversight

Eversight — FEI 3000718321

The FDA completed an inspection of Eversight on September 28, 2017 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
September 28, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Ann Arbor, MI (United States)