# FDA Inspection 1291320 - Moximed, Inc. - October 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/moximed-inc/407795ad-aab2-4107-9c27-82448448601c
Source feed: FDA_Inspections

> FDA Inspection 1291320 for Moximed, Inc. on October 28, 2025. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1291320
- Company Name: Moximed, Inc.
- Inspection Date: 2025-10-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1291320 - 2025-10-28](https://www.keypedia.com/records/fda_inspections/moximed-inc/03ca9d1b-fdb6-4508-a2ab-7e8ddafe21ff)
- [FDA Inspection 1291320 - 2025-10-28](https://www.keypedia.com/records/fda_inspections/moximed-inc/7308b213-05b3-4877-ad47-ac7480bd3022)
- [FDA Inspection 1019036 - 2017-07-07](https://www.keypedia.com/records/fda_inspections/moximed-inc/b1e6d9c4-ab12-43d8-9a88-da5519f9ecd7)

Company: https://www.keypedia.com/companies/moximed-inc/68a32f9f-4a0f-4769-8dba-27d139a81f5b

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