FDA Inspection 992059 — Vertos Medical, Inc.

Vertos Medical, Inc. — FEI 3006450448

The FDA completed an inspection of Vertos Medical, Inc. on November 10, 2016 in Aliso Viejo, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 10, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Aliso Viejo, CA (United States)