# FDA Inspection 1244590 - KDI Med Supply - July 15, 2024

Source: https://www.keypedia.com/records/fda_inspections/kdi-med-supply/d3ce249a-ad4b-4403-a641-57126f0a08f8
Source feed: FDA_Inspections

> FDA Inspection 1244590 for KDI Med Supply on July 15, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1244590
- Company Name: KDI Med Supply
- Inspection Date: 2024-07-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1244590 - 2024-07-15](https://www.keypedia.com/records/fda_inspections/kdi-med-supply/758439d0-0911-43f9-98c9-adf06c0903a9)

Company: https://www.keypedia.com/companies/kdi-med-supply/9f10bf35-6258-4748-b92d-5fe682e7a5f2

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