FDA Inspection 1017583 — Neuroptics Inc

Neuroptics Inc — FEI 3004185638

The FDA completed an inspection of Neuroptics Inc on May 25, 2017 in Irvine, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 25, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)