LISI MEDICAL Remmele, Inc.

Form 483FOIA Uncovered

Coon Rapids, Minnesota, United StatesFEI 3000203391Issued July 12, 2022

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 3000203391.

Observations2

Issue DateJuly 12, 2022

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: LISI MEDICAL Remmele, Inc.
Location: Coon Rapids, Minnesota, United States
FEI Number: 3000203391
Product Type: Devices
Issue Date: July 12, 2022
Country: United States

Inspection History, 2009 to 2025

NAI3

VAI2

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

Act on This Form 483

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LISI MEDICAL Remmele, Inc. FDA Form 483, Coon Rapids, Minnesota, July 12, 2022