FDA Inspection 1102759 — LG Electronics Inc.

LG Electronics Inc. — FEI 1000622248

The FDA completed an inspection of LG Electronics Inc. on June 10, 2019 in Tianjin. 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
June 10, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Tianjin (China)