FDA Inspection 1094122 — Syntech International, Inc

Syntech International, Inc — FEI 3005142514

The FDA completed an inspection of Syntech International, Inc on May 9, 2019 in Irvine, 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
May 9, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)