FDA Inspection 962189 — IPAX, Incorporated

IPAX, Incorporated — FEI 1720734

The FDA completed an inspection of IPAX, Incorporated on March 2, 2016 in Englewood, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 2, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Englewood, CO (United States)

Citations

IDCFRDescription
312821 CFR 820.90(a)Nonconforming product control
313021 CFR 820.100(a)Lack of or inadequate procedures