# Nihon Kohden America LLC - Inspection Records

Source: https://www.keypedia.com/companies/nihon-kohden-america-llc/6d634199-3448-4668-ae42-2ca3ea095b6a

> Inspection records and compliance data for Nihon Kohden America LLC in Irvine, California. Access full analysis and detailed observations.

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## Details

- Name: Nihon Kohden America LLC
- FEI Number: 2080783
- City: Irvine
- State: California
- Country Name: United States
- Address Line 1: 15353 Barranca Pkwy
- Zip Code: 92618

## Related Documents

- [FDA Inspection 1252486 - Nihon Kohden America LLC - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/345c2181-1220-48e5-9d10-8f7bc9615807) — source: FDA, date: October 4, 2024
- [FDA Inspection 1252486 - Nihon Kohden America LLC - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/b7c73937-488a-475c-91d9-1adda8869bbb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 4, 2024
- [FDA Inspection 1252486 - Nihon Kohden America LLC - 2024-10-04](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/1f281d46-cbc6-4216-aec3-143313a2337f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 4, 2024
- [FDA Inspection 1142130 - Nihon Kohden America LLC - 2021-05-03](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/e80a9dda-c86b-43bf-bd24-db5805922bc0) — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2021
- [FDA Inspection 1142130 - Nihon Kohden America LLC - 2021-05-03](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/e0e8869c-7832-447d-a465-4e1c9da1c8c4) — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2021
- [483 - Nihon Kohden America LLC - 2019-04-30](https://www.keypedia.com/records/483/nihon-kohden-america-llc/3b2c1099-94c8-4bdb-8edb-734c424e3f37) — source: FDA, date: April 30, 2019
- [FDA Inspection 1088972 - Nihon Kohden America LLC - 2019-04-30](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/b95e490b-83a8-4ea8-915f-659ea44130e9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 30, 2019
- [FDA Inspection 1088972 - Nihon Kohden America LLC - 2019-04-30](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/715540c2-32fb-44bd-b143-9643c4e99bb2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 30, 2019
- [FDA Inspection 1040786 - Nihon Kohden America LLC - 2017-10-26](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/85329d9b-a18d-489e-a59a-db67c884e67a) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2017
- [FDA Inspection 1040786 - Nihon Kohden America LLC - 2017-10-26](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/ec0effbe-7583-4a4f-96d8-246783364bbd) — classification: No Action Indicated (NAI), source: FDA, date: October 26, 2017
- [FDA Inspection 876623 - Nihon Kohden America LLC - 2014-04-24](https://www.keypedia.com/records/fda_inspections/nihon-kohden-america-llc/409c33ea-cf30-4605-bf72-14655b179ed3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2014

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