FDA Inspection 986370 — Eyegaze Inc.

Eyegaze Inc. — FEI 1000123308

The FDA completed an inspection of Eyegaze Inc. on Sep 15, 2016 in Fairfax, 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
Sep 15, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Fairfax, VA (United States)

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