Keller Laboratories

Form 483

Fenton, Missouri, United StatesFEI 3006650414Issued February 11, 2011

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 3006650414.

Observations5

Issue DateFebruary 11, 2011

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Keller Laboratories
Location: Fenton, Missouri, United States
FEI Number: 3006650414
Product Type: Devices
Issue Date: February 11, 2011
Country: United States

Inspection History, 2011 to 2023

NAI1

VAI4

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

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Keller Laboratories FDA Form 483, Fenton, Missouri, February 11, 2011