# FDA Inspection 1024289 - LG Electronics Inc. - May 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/8bc781d0-5966-4fb7-ab6a-aa902523b6ca
Source feed: FDA_Inspections

> FDA Inspection 1024289 for LG Electronics Inc. on May 10, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1024289
- Company Name: LG Electronics Inc.
- Inspection Date: 2017-05-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1259899 - 2024-11-07](https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/0045dd60-a428-46d1-b4ef-345b5fd0a919)
- [FDA Inspection 1102759 - 2019-06-10](https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/93831304-178e-4299-8530-dd008d267a81)
- [FDA Inspection 935021 - 2015-06-24](https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/72c30a09-460d-458e-ae5f-173f7ed30850)
- [FDA Inspection 666785 - 2010-05-18](https://www.keypedia.com/records/fda_inspections/lg-electronics-inc/6ea3f3d5-f4f0-4931-95b0-392e1cc8d4f0)

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