# FDA Inspection 1237790 - IntelleWave, Inc. - April 25, 2024

Source: https://www.keypedia.com/records/fda_inspections/intellewave-inc/75a8cceb-33c4-49d7-a128-892def958e8e
Source feed: FDA_Inspections

> FDA Inspection 1237790 for IntelleWave, Inc. on April 25, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1237790
- Company Name: IntelleWave, Inc.
- Inspection Date: 2024-04-25
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1237790 - 2024-04-25](https://www.keypedia.com/records/fda_inspections/intellewave-inc/0ba23687-52df-403b-9a3f-0598a3d9be80)
- [FDA Inspection 1020784 - 2017-08-02](https://www.keypedia.com/records/fda_inspections/intellewave-inc/6a9174c4-313a-4749-9d9d-9e2103700391)

Company: https://www.keypedia.com/companies/intellewave-inc/77dd1263-9e8d-4924-9f19-5ca88ef1849c

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