FDA Inspection 1187537 — Intechrity Inc

Intechrity Inc — FEI 3009887154

The FDA completed an inspection of Intechrity Inc on October 27, 2022 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
October 27, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)