# FDA Inspection 1288112 - MEMED US INC. - September 30, 2025

Source: https://www.keypedia.com/records/fda_inspections/memed-us-inc/3add64ce-b82e-4616-a041-5ce03e6c7f2f
Source feed: FDA_Inspections

> FDA Inspection 1288112 for MEMED US INC. on September 30, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288112
- Company Name: MEMED US INC.
- Inspection Date: 2025-09-30
- 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 1288112 - 2025-09-30](https://www.keypedia.com/records/fda_inspections/memed-us-inc/4fd9912d-5bcb-4315-a7b5-b3ad4dee3efd)
- [FDA Inspection 1288112 - 2025-09-30](https://www.keypedia.com/records/fda_inspections/memed-us-inc/039b8097-065e-4cd2-9161-c9059faf8334)

Company: https://www.keypedia.com/companies/memed-us-inc/5d7a8253-2a5b-4365-ad66-17b45193dd57

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