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FDA Inspection 1085161 — Euclid Vision Corporation

Euclid Vision Corporation — FEI 3014175039

The FDA completed an inspection of Euclid Vision Corporation on Feb 21, 2019 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
Feb 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sterling, VA (United States)

Facility

Other inspections at this facility

FDA data resources

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