# FDA Inspection 1180750 - Endoplus - September 08, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/endoplus/de9b6790-4b65-4fae-beb3-2a1840b288b8
Source feed: FDA_Inspections

> FDA Inspection 1180750 for Endoplus on September 08, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1180750
- Company Name: Endoplus
- Inspection Date: 2022-09-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1307460 - 2026-02-25](https://www.globalkeysolutions.net/records/fda_inspections/endoplus/13e205a4-f0f7-4465-8e05-f229306bb561)
- [FDA Inspection 1307460 - 2026-02-25](https://www.globalkeysolutions.net/records/fda_inspections/endoplus/3020a70d-1ab9-4cec-8cf0-f7efbcd1e4ad)
- [FDA Inspection 1307460 - 2026-02-25](https://www.globalkeysolutions.net/records/fda_inspections/endoplus/c090cffa-6740-4756-aab2-d90c1c538e28)
- [FDA Inspection 1180750 - 2022-09-08](https://www.globalkeysolutions.net/records/fda_inspections/endoplus/e36a94f3-41a9-442c-b9bb-551f636f2ea8)
- [FDA Inspection 1022171 - 2017-08-02](https://www.globalkeysolutions.net/records/fda_inspections/endoplus/bbc7328d-3612-447a-8922-ee6fa95f5617)

Company: https://www.globalkeysolutions.net/companies/endoplus/9145c0d3-d056-483a-93f5-f588957afd2a

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7