# Endoplus - Inspection Records

Source: https://www.keypedia.com/companies/endoplus/9145c0d3-d056-483a-93f5-f588957afd2a

> Inspection records and compliance data for Endoplus in Mundelein, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Endoplus
- FEI Number: 3000719482
- City: Mundelein
- State: Illinois
- Country Name: United States
- Address Line 1: 750 Tower Rd Ste A
- Zip Code: 60060

## Related Documents

- [FDA Inspection 1307460 - Endoplus - 2026-02-25](https://www.keypedia.com/records/fda_inspections/endoplus/13e205a4-f0f7-4465-8e05-f229306bb561) — source: FDA, date: February 25, 2026
- [FDA Inspection 1307460 - Endoplus - 2026-02-25](https://www.keypedia.com/records/fda_inspections/endoplus/3020a70d-1ab9-4cec-8cf0-f7efbcd1e4ad) — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2026
- [FDA Inspection 1307460 - Endoplus - 2026-02-25](https://www.keypedia.com/records/fda_inspections/endoplus/c090cffa-6740-4756-aab2-d90c1c538e28) — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2026
- [FDA Inspection 1180750 - Endoplus - 2022-09-08](https://www.keypedia.com/records/fda_inspections/endoplus/e36a94f3-41a9-442c-b9bb-551f636f2ea8) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2022
- [FDA Inspection 1180750 - Endoplus - 2022-09-08](https://www.keypedia.com/records/fda_inspections/endoplus/de9b6790-4b65-4fae-beb3-2a1840b288b8) — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2022
- [FDA Inspection 1022171 - Endoplus - 2017-08-02](https://www.keypedia.com/records/fda_inspections/endoplus/71d73bf0-c823-4faa-a26c-1a7d8592d08e) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2017
- [FDA Inspection 1022171 - Endoplus - 2017-08-02](https://www.keypedia.com/records/fda_inspections/endoplus/bbc7328d-3612-447a-8922-ee6fa95f5617) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2017
- [FDA Inspection 926048 - Endoplus - 2015-05-19](https://www.keypedia.com/records/fda_inspections/endoplus/fb5ddfe5-2517-4b86-b6b0-8dd5a69c66de) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 19, 2015
- [FDA Inspection 926048 - Endoplus - 2015-05-19](https://www.keypedia.com/records/fda_inspections/endoplus/5bd6d364-4965-4a04-99dc-d2448aebd67f) — classification: No Action Indicated (NAI), source: FDA, date: May 19, 2015
- [FDA Inspection 820624 - Endoplus - 2013-02-26](https://www.keypedia.com/records/fda_inspections/endoplus/5b2df8e1-684e-44f2-a141-cd7a6bfdf961) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 26, 2013

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