FDA Inspection 747017 — Apixia Inc

Apixia Inc — FEI 3008361230

The FDA completed an inspection of Apixia Inc on September 7, 2011 in City Of Industry, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
City Of Industry, CA (United States)

Citations

IDCFRDescription
63021 CFR 803.17Lack of Written MDR Procedures