# LG Electronics Inc. – FDA Inspection, Jun 24, 2015

Source: https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/72c30a09-460d-458e-ae5f-173f7ed30850
Source feed: FDA_Inspections

> FDA inspection 935021 of LG Electronics Inc., June 24, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 1030. 4 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 935021
- Company Name: LG Electronics Inc.
- Inspection Date: 2015-06-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1259899 - 2024-11-07
- FDA Inspection 1102759 - 2019-06-10
- [FDA Inspection 1024289 - 2017-05-10](https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/8bc781d0-5966-4fb7-ab6a-aa902523b6ca)
- FDA Inspection 666785 - 2010-05-18

Company: https://www.keypedia.com/companies/lg-electronics-inc/2078f2b1-4cef-400d-ac2e-128121305c6a

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7