FDA Inspection 935021 — LG Electronics Inc.
The FDA completed an inspection of LG Electronics Inc. on June 24, 2015 in Tianjin. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 24, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Tianjin (China)
Citations
| ID | CFR | Description |
|---|---|---|
| 5940 | 21 CFR 1030.10(c)(3)(i) | tests--errors and uncertainties accounted for |