# LG Electronics Inc. – FDA Inspection, 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 of LG Electronics Inc., May 10, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 1010 and 1030. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024289
- Company Name: LG Electronics Inc.
- Inspection Date: 2017-05-10
- 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: 2

## Related Documents

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- [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

## Related Officers

- Issuing Officer
- Issuing Officer

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