# Gynex Corporation - Inspection Records

Source: https://www.keypedia.com/companies/gynex-corporation/3320db3d-b0e6-4488-8161-0265bdcd9b4d

> Inspection records and compliance data for Gynex Corporation in Redmond, Washington. Access full analysis and detailed observations.

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## Details

- Name: Gynex Corporation
- FEI Number: 3001238683
- City: Redmond
- State: Washington
- Country Name: United States
- Address Line 1: 14603 NE 87th St
- Zip Code: 98052

## Related Documents

- [483 - Gynex Corporation - 2020-01-06](https://www.keypedia.com/records/483/gynex-corporation/ac29ccfd-7f5c-45d6-ab75-ab6e7677126d) — source: FDA, date: January 6, 2020
- [FDA Inspection 1114673 - Gynex Corporation - 2020-01-06](https://www.keypedia.com/records/fda_inspections/gynex-corporation/eb7b1b53-6387-4585-865f-87329d37c128) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 6, 2020
- [FDA Inspection 1114673 - Gynex Corporation - 2020-01-06](https://www.keypedia.com/records/fda_inspections/gynex-corporation/12296a52-e5af-4b04-964c-dcc1d82ae3e3) — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2020
- [FDA Inspection 975324 - Gynex Corporation - 2016-05-27](https://www.keypedia.com/records/fda_inspections/gynex-corporation/323a2be2-ed3b-4148-abe3-d5ca52a18a0b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 27, 2016
- [FDA Inspection 975324 - Gynex Corporation - 2016-05-27](https://www.keypedia.com/records/fda_inspections/gynex-corporation/a188bf29-d209-4c68-b1ba-d4f174b39148) — classification: No Action Indicated (NAI), source: FDA, date: May 27, 2016
- [FDA Inspection 876242 - Gynex Corporation - 2014-04-25](https://www.keypedia.com/records/fda_inspections/gynex-corporation/b6be5851-24d7-42a7-9231-93fa094bff22) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 25, 2014
- [FDA Inspection 876242 - Gynex Corporation - 2014-04-25](https://www.keypedia.com/records/fda_inspections/gynex-corporation/eb6ce85d-3da2-448c-bebe-00acefa7ef2d) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2014
- [FDA Inspection 800085 - Gynex Corporation - 2012-09-21](https://www.keypedia.com/records/fda_inspections/gynex-corporation/fe90ccad-a7fd-47a2-b5c0-4c088d755c06) — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2012
- [FDA Inspection 791097 - Gynex Corporation - 2012-07-20](https://www.keypedia.com/records/fda_inspections/gynex-corporation/7b7bd45d-f5fa-4deb-9053-21e5123d8e5d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 20, 2012
- [FDA Inspection 791097 - Gynex Corporation - 2012-07-20](https://www.keypedia.com/records/fda_inspections/gynex-corporation/59aa9f87-4405-49dc-83d8-b17d3dcec35b) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2012
- [FDA Inspection 645081 - Gynex Corporation - 2010-01-21](https://www.keypedia.com/records/fda_inspections/gynex-corporation/18210e64-b7e7-477d-865f-373835c77fe7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 21, 2010

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