# FDA Inspection 1256347 - I/O Urology Corporation - October 30, 2024

Source: https://www.keypedia.com/records/fda_inspections/io-urology-corporation/850063e8-d8c6-4d4f-8c4e-d882da769a5c
Source feed: FDA_Inspections

> FDA Inspection 1256347 for I/O Urology Corporation on October 30, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1256347
- Company Name: I/O Urology Corporation
- Inspection Date: 2024-10-30
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1256347 - 2024-10-30](https://www.keypedia.com/records/fda_inspections/io-urology-corporation/1da0bb7a-3659-41cd-b4a8-767fc538b81f)
- [FDA Inspection 1256347 - 2024-10-30](https://www.keypedia.com/records/fda_inspections/io-urology-corporation/7cb3d8b8-9344-4d01-a114-7217b7c9edac)

Company: https://www.keypedia.com/companies/io-urology-corporation/70eacad0-f913-4d10-8ce3-c3a56542c8c9

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