# FDA Inspection 1204008 - IntriCon Corp - April 17, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/intricon-corp/dc9721b5-36e5-40b9-a52e-d005da47c2ab
Source feed: FDA_Inspections

> FDA Inspection 1204008 for IntriCon Corp on April 17, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1204008
- Company Name: IntriCon Corp
- Inspection Date: 2023-04-17
- 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 1204008 - 2023-04-17](https://www.globalkeysolutions.net/records/fda_inspections/intricon-corp/379b6334-91c4-4989-9100-ce92921af622)
- [FDA Inspection 1041021 - 2017-12-19](https://www.globalkeysolutions.net/records/fda_inspections/intricon-corp/0b742043-ffee-4069-9783-051d7eca42b3)
- [FDA Inspection 859967 - 2013-12-17](https://www.globalkeysolutions.net/records/fda_inspections/intricon-corp/b3ded3d9-3f9b-4bc8-b64e-9b860fe46d8e)

Company: https://www.globalkeysolutions.net/companies/intricon-corp/39f0e161-9706-4084-a255-3bde3210ecf5

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