Koven Technology, Inc.

Form 483

Saint Louis, Missouri, United StatesFEI 1937397Issued November 03, 2017

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 1937397.

Observations1

Issue DateNovember 03, 2017

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Koven Technology, Inc.
Location: Saint Louis, Missouri, United States
FEI Number: 1937397
Product Type: Devices
Issue Date: November 03, 2017
Country: United States

Inspection History, 2017 to 2026

NAI2

VAI1

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

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Koven Technology, Inc. FDA Form 483, Saint Louis, Missouri, November 3, 2017