FDA Inspection 904628 — Shenzhen Pango Electronic Co., Ltd

Shenzhen Pango Electronic Co., Ltd — FEI 3006792041

The FDA completed an inspection of Shenzhen Pango Electronic Co., Ltd on Nov 13, 2014 in Shenzhen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 13, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Shenzhen (China)