LG Electronics Inc., Tianjin, China – FDA Inspections

Inspection records and compliance data for LG Electronics Inc. in Tianjin. 5 FDA inspections on record, 1 Form 483, last inspected November 07, 2024.

Company Profile

This profile covers LG Electronics Inc. based in Tianjin, China.

FDA Inspection History

FDA inspections: 5
OAI: 0
VAI: 2
NAI: 3
Form 483s: 1
Warning letters: 0

First inspected May 18, 2010. Last inspected November 7, 2024.

Most cited issue areas

Certification not based on adequate test/testing program1 inspection
Means to monitor interlocks1 inspection
tests--errors and uncertainties accounted for1 inspection

FDA inspections (5)

Date	Result	FDA center(s)	Insp. #
November 7, 2024	NAI	Medical Devices & Rad Health · Radiation Control and Health Safety Act	1259899
June 10, 2019	NAI	Medical Devices & Rad Health · Radiation Control and Health Safety Act	1102759
May 10, 2017	VAI	Medical Devices & Rad Health · Radiation Control and Health Safety Act	1024289
June 24, 2015	VAI	Medical Devices & Rad Health · Radiation Control and Health Safety Act	935021
May 18, 2010	NAI	Medical Devices & Rad Health · Radiation Control and Health Safety Act	666785

FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

Advanced Technology Laser Co., Ltd.

Guangzhou Berrcom Medical Device Co., Ltd

Suzhou Armocon Technology Co.Ltd

Sejoy Electronics & Instruments Co. LTD.

SHENZHEN SIJIAHUA TECHNOLOGY LTD

Assure Tech (Hangzhou) Co., Ltd

IDT Electronics (Shenzhen) Co., Ltd.

DELIFENG ELECTRONICS (SHENZHEN) CO., LTD.

Shenzhen Superwave Laser Technology Co. Ltd.

SUNTECH MEDICAL DEVICES (SHENZHEN) CO., LTD.