# PixxGen Corporation - Inspection Records

Source: https://www.globalkeysolutions.net/companies/pixxgen-corporation/39aa3bc5-2ef8-4057-8b97-f293d43b4d47

> Inspection records and compliance data for PixxGen Corporation in Anyang, None. Access full analysis and detailed observations.

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## Details

- Name: PixxGen Corporation
- FEI Number: 3008164200
- City: Anyang
- State: None
- Country Name: Korea (the Republic of)
- Address Line 1: 5f, Smart Bay, 123, Beolmal-Ro, Dongan-Gu
- Zip Code: None

## Related Documents

- [FDA Inspection 1116209 - PixxGen Corporation - 2020-01-16](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/e099d52e-7fe1-4fe0-ae68-62bea30dea4a) — classification: Official Action Indicated (OAI), source: FDA, date: January 16, 2020
- [FDA Inspection 1116209 - PixxGen Corporation - 2020-01-16](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/ecf8a518-30a0-483c-a1bc-141afe7ad969) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 16, 2020
- [FDA Inspection 1116209 - PixxGen Corporation - 2020-01-16](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/df4004dc-a39f-4320-8286-08cdb73b1d97) — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2020
- [FDA Inspection 841196 - PixxGen Corporation - 2013-06-26](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/d27238e4-ea64-45ef-ae6b-453869325f02) — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2013
- [FDA Inspection 841196 - PixxGen Corporation - 2013-06-26](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/9c8e1a01-5b9d-4178-8c1a-8d39b650e89a) — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2013
- [FDA Inspection 841196 - PixxGen Corporation - 2013-06-26](https://www.globalkeysolutions.net/records/fda_inspections/pixxgen-corporation/22c846e5-31a7-449e-918b-88689d60c341) — classification: No Action Indicated (NAI), source: FDA, date: June 26, 2013

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