# FDA Inspection 1098182 - Neomedix Corporation - June 19, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/neomedix-corporation/b3214a98-027e-43c8-beb7-2a37cada63ff
Source feed: FDA_Inspections

> FDA Inspection 1098182 for Neomedix Corporation on June 19, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1098182
- Company Name: Neomedix Corporation
- Inspection Date: 2019-06-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1098182 - 2019-06-19](https://www.globalkeysolutions.net/records/fda_inspections/neomedix-corporation/4be46570-9025-42d3-a683-492f9b0c0a54)
- [FDA Inspection 1047029 - 2018-03-29](https://www.globalkeysolutions.net/records/fda_inspections/neomedix-corporation/d4346570-ae2d-4318-9e89-2f29cc46695d)
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- [FDA Inspection 896544 - 2014-09-19](https://www.globalkeysolutions.net/records/fda_inspections/neomedix-corporation/a3dd7d04-7c75-4862-a149-91f650e5efea)
- [FDA Inspection 896544 - 2014-09-19](https://www.globalkeysolutions.net/records/fda_inspections/neomedix-corporation/0db705d5-3a93-4eec-b524-9365ca9c7ccf)

Company: https://www.globalkeysolutions.net/companies/neomedix-corporation/4c7ebf26-90bd-4090-9d8d-12b641ea60a5

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