FDA Inspection 857368 — Phoenix Deventures

Phoenix Deventures — FEI 3008514120

The FDA completed an inspection of Phoenix Deventures on December 6, 2013 in Morgan Hill, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 6, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Morgan Hill, CA (United States)

Citations

IDCFRDescription
331021 CFR 820.120(b)DHR documentation of label release {see also 820.184}
369621 CFR 820.100(b)Documentation