# FDA Inspection 1306740 - Evoendo, Inc. - March 02, 2026

Source: https://www.keypedia.com/records/fda_inspections/evoendo-inc/b33be43b-a407-4dba-afe6-ea2ae97ad3e0
Source feed: FDA_Inspections

> FDA Inspection 1306740 for Evoendo, Inc. on March 02, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1306740
- Company Name: Evoendo, Inc.
- Inspection Date: 2026-03-02
- 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 1306740 - 2026-03-02](https://www.keypedia.com/records/fda_inspections/evoendo-inc/7489650b-19bf-43e4-8624-d09dc06620cb)
- [FDA Inspection 1306740 - 2026-03-02](https://www.keypedia.com/records/fda_inspections/evoendo-inc/30d9a114-2468-4d98-84e8-d9fa641dfb78)

Company: https://www.keypedia.com/companies/evoendo-inc/2828633f-92b4-4942-af74-c42ac9200921

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