FDA Inspection 1016867 — Sanzay Corporation

Sanzay Corporation — FEI 3005146313

The FDA completed an inspection of Sanzay Corporation on April 13, 2017 in Hialeah, FL. 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
April 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Hialeah, FL (United States)