Kinetic Instruments, Inc.

Form 483

Bethel, Connecticut, United StatesFEI 1294153Issued January 06, 2016

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 1294153.

Observations2

Issue DateJanuary 06, 2016

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: Kinetic Instruments, Inc.
Location: Bethel, Connecticut, United States
FEI Number: 1294153
Product Type: Devices
Issue Date: January 06, 2016
Country: United States

Inspection History, 2016 to 2019

NAI1

VAI1

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

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Kinetic Instruments, Inc. FDA Form 483, Bethel, Connecticut, January 6, 2016