Reprise Biomedical, Inc.

Form 483

Plymouth, Minnesota, United StatesFEI 3010894343Issued November 20, 2025

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3010894343.

Observations1

Issue DateNovember 20, 2025

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Reprise Biomedical, Inc.
Location: Plymouth, Minnesota, United States
FEI Number: 3010894343
Product Type: Devices
Issue Date: November 20, 2025
Country: United States

Inspection History, 2015 to 2025

NAI2

VAI2

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

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Reprise Biomedical, Inc. FDA Form 483, Plymouth, Minnesota, November 20, 2025