# FDA Inspection 1250821 - 410 Medical, Inc. - August 16, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/410-medical-inc/903a5dab-c2b7-4e35-8407-2e18d39b8158
Source feed: FDA_Inspections

> FDA Inspection 1250821 for 410 Medical, Inc. on August 16, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250821
- Company Name: 410 Medical, Inc.
- Inspection Date: 2024-08-16
- 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 1250821 - 2024-08-16](https://www.globalkeysolutions.net/records/fda_inspections/410-medical-inc/941fcb87-f860-41bf-af25-d269863dd756)
- [FDA Inspection 1120620 - 2020-03-12](https://www.globalkeysolutions.net/records/fda_inspections/410-medical-inc/2a113a47-cc18-4811-827e-4fecd53440a9)
- [FDA Inspection 1120620 - 2020-03-12](https://www.globalkeysolutions.net/records/fda_inspections/410-medical-inc/9bba290b-5461-451d-b172-de6e1812d4b6)

Company: https://www.globalkeysolutions.net/companies/410-medical-inc/20383801-3734-485f-9de7-f31ccbd51556

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