Aprios Custom Mfg

Form 483

Minneapolis, Minnesota, United StatesFEI 3004612223Issued February 07, 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 3004612223.

Observations1

Issue DateFebruary 07, 2025

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Aprios Custom Mfg
Location: Minneapolis, Minnesota, United States
FEI Number: 3004612223
Product Type: Devices
Issue Date: February 07, 2025
Country: United States

Inspection History, 2014 to 2025

NAI3

VAI1

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

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Aprios Custom Mfg FDA Form 483, Minneapolis, Minnesota, February 7, 2025