FDA Inspection 843271 — SunMed AP, Ltd.

SunMed AP, Ltd. — FEI 3005998497

The FDA completed an inspection of SunMed AP, Ltd. on May 30, 2013 in Zhuhai. 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 30, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Zhuhai (China)