# Reprise Biomedical, Inc. - Inspection Records

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

> Inspection records and compliance data for Reprise Biomedical, Inc. in Plymouth, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Reprise Biomedical, Inc.
- FEI Number: 3010894343
- City: Plymouth
- State: Minnesota
- Country Name: United States
- Address Line 1: 17400 Medina Rd Ste 100
- Zip Code: 55447

## Related Documents

- [483 - Reprise Biomedical, Inc. - 2025-11-20](https://www.keypedia.com/records/483/reprise-biomedical-inc/dd30f6d6-5ce4-4a26-affd-1e0479df319a) — source: FDA, date: November 20, 2025
- [FDA Inspection 1292234 - Reprise Biomedical, Inc. - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/5e4bd7e0-77f4-4579-be02-01946db73ea2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2025
- [FDA Inspection 1292234 - Reprise Biomedical, Inc. - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/1b63b727-dbf3-4338-96df-963436576142) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2025
- [FDA Inspection 1292234 - Reprise Biomedical, Inc. - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/3d6cde12-ab34-4913-bbef-81e87dd2dfb9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2025
- [FDA Inspection 1292234 - Reprise Biomedical, Inc. - 2025-11-20](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/445f6e75-706e-4148-a5f0-1998ed956c6f) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2025
- [FDA Inspection 1146260 - Reprise Biomedical, Inc. - 2021-07-08](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/2cb16fb7-0db2-45cd-b753-26937d359d97) — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2021
- [FDA Inspection 1146260 - Reprise Biomedical, Inc. - 2021-07-08](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/a79a56d6-6dd8-4e14-b6e3-664663f1706f) — classification: No Action Indicated (NAI), source: FDA, date: July 8, 2021
- [FDA Inspection 1085602 - Reprise Biomedical, Inc. - 2019-04-02](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/67cd3518-e0ef-4976-8217-3cad129a4ad2) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2019
- [FDA Inspection 1085602 - Reprise Biomedical, Inc. - 2019-04-02](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/3235fa66-5f3c-4b7f-bd43-4758d935a9f8) — classification: No Action Indicated (NAI), source: FDA, date: April 2, 2019
- [FDA Inspection 943066 - Reprise Biomedical, Inc. - 2015-09-18](https://www.keypedia.com/records/fda_inspections/reprise-biomedical-inc/c780991b-671a-4042-8667-025451991887) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 18, 2015

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