FDA Inspection
LG Electronics Inc.LG Electronics Inc. – FDA Inspection, Jun 24, 2015
Record Details
This FDA Inspection record concerns LG Electronics Inc., with an inspection on June 24, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LG Electronics Inc.
- Inspection Date
- June 24, 2015
- Product Type
- Devices
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ID · 72c30a09-460d-458e-ae5f-173f7ed30850
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 935021
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
1- 21 CFR 1030.10(c)(3)(i)tests--errors and uncertainties accounted for
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Other FDA inspections of LG Electronics Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| November 7, 2024 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| June 10, 2019 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 10, 2017 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| May 18, 2010 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for LG Electronics Inc.
- FDA Inspection 1259899 - 2024-11-07
- FDA Inspection 1102759 - 2019-06-10
- FDA Inspection 1024289 - 2017-05-10
- FDA Inspection 666785 - 2010-05-18
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