# FDA Inspection 1194164 - InfoBionic, Inc. - November 17, 2022

Source: https://www.keypedia.com/records/fda_inspections/infobionic-inc/efb9d426-dbe9-4a7a-aed5-7f67b7503137
Source feed: FDA_Inspections

> FDA Inspection 1194164 for InfoBionic, Inc. on November 17, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1194164
- Company Name: InfoBionic, Inc.
- Inspection Date: 2022-11-17
- 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 1194164 - 2022-11-17](https://www.keypedia.com/records/fda_inspections/infobionic-inc/13c17930-f253-40b4-9de2-0f1ce59deffa)
- [FDA Inspection 1085891 - 2019-04-10](https://www.keypedia.com/records/fda_inspections/infobionic-inc/6a7ac35e-65eb-4746-8edb-fad7dd913be3)

Company: https://www.keypedia.com/companies/infobionic-inc/eacb0491-ba47-41dd-bfef-0b0062c9d473

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