# FDA Inspection 1085602 - Reprise Biomedical, Inc. - April 02, 2019

Source: https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/67cd3518-e0ef-4976-8217-3cad129a4ad2
Source feed: FDA_Inspections

> FDA Inspection 1085602 for Reprise Biomedical, Inc. on April 02, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1085602
- Company Name: Reprise Biomedical, Inc.
- Inspection Date: 2019-04-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1292234 - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/1b63b727-dbf3-4338-96df-963436576142)
- [FDA Inspection 1292234 - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/5e4bd7e0-77f4-4579-be02-01946db73ea2)
- [FDA Inspection 1292234 - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/445f6e75-706e-4148-a5f0-1998ed956c6f)
- [FDA Inspection 1292234 - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/3d6cde12-ab34-4913-bbef-81e87dd2dfb9)
- [FDA Inspection 1146260 - 2021-07-08](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/2cb16fb7-0db2-45cd-b753-26937d359d97)

Company: https://www.keypedia.com/companies/reprise-biomedical-inc/6eef21a0-954c-42b0-ac0a-f7bda7b31f0f

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