FDA Inspection 1014716 — Phoenix Deventures

Phoenix Deventures — FEI 3008514120

The FDA completed an inspection of Phoenix Deventures on May 4, 2017 in Morgan Hill, 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
May 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Morgan Hill, CA (United States)