# FDA Inspection 987599 - ihear Medical Inc. - September 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/ihear-medical-inc/7b714b73-fdfa-48da-aed2-5928053aed32
Source feed: FDA_Inspections

> FDA Inspection 987599 for ihear Medical Inc. on September 22, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987599
- Company Name: ihear Medical Inc.
- Inspection Date: 2016-09-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 987599 - 2016-09-22](https://www.keypedia.com/records/fda_inspections/ihear-medical-inc/219dd51e-f1f6-42a9-a7ea-ed3578bb3698)

Company: https://www.keypedia.com/companies/ihear-medical-inc/e58b5cd0-fe90-45ce-8dc0-548910ffbd89

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