FDA Inspection 1068726 — IPAX, Incorporated

IPAX, Incorporated — FEI 1720734

The FDA completed an inspection of IPAX, Incorporated on October 11, 2018 in Englewood, CO. 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 11, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Englewood, CO (United States)