FDA Inspection 1018730 — Vivax Medical Corp.

Vivax Medical Corp. — FEI 1000513669

The FDA completed an inspection of Vivax Medical Corp. on July 14, 2017 in Naugatuck, CT. 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
July 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Naugatuck, CT (United States)