# FDA Inspection 1299822 - MIDWAY MEDICAL - January 15, 2026

Source: https://www.keypedia.com/records/fda_inspections/midway-medical/05fe843e-31ab-4658-8bb3-bb9eca054875
Source feed: FDA_Inspections

> FDA Inspection 1299822 for MIDWAY MEDICAL on January 15, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1299822
- Company Name: MIDWAY MEDICAL
- Inspection Date: 2026-01-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Chicago District Office

## Related Documents

- [FDA Inspection 1299822 - 2026-01-15](https://www.keypedia.com/records/fda_inspections/midway-medical/36bcd68e-8e09-479e-948f-f47984210f8b)
- [FDA Inspection 1299822 - 2026-01-15](https://www.keypedia.com/records/fda_inspections/midway-medical/0ec7874c-b704-425b-8bab-8cedfb06268e)
- [FDA Inspection 1299822 - 2026-01-15](https://www.keypedia.com/records/fda_inspections/midway-medical/17dba52c-0190-462b-a918-64883a7fa639)

Company: https://www.keypedia.com/companies/midway-medical/d03a5807-9714-4bd8-9826-b4c84d6f3980

Office: https://www.keypedia.com/offices/chicago-district-office/a510300b-0eaf-4a33-90b5-231d95977669