FDA Inspection 1043716 — Euclid Vision Corporation

Euclid Vision Corporation — FEI 3014175039

The FDA completed an inspection of Euclid Vision Corporation on Mar 7, 2018 in Sterling, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sterling, VA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.