Weiman Products, LLC

Form 483FOIA Uncovered

Gurnee, Illinois, United StatesFEI 1416404Issued January 10, 2018

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 1416404.

Observations1

Issue DateJanuary 10, 2018

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Weiman Products, LLC
Location: Gurnee, Illinois, United States
FEI Number: 1416404
Product Type: Devices
Issue Date: January 10, 2018
Country: United States

Inspection History, 2015 to 2026

NAI1

VAI2

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

Act on This Form 483

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Weiman Products, LLC FDA Form 483, Gurnee, Illinois, January 10, 2018