Chitogen, Inc.

Form 483

Plymouth, Minnesota, United StatesFEI 3007788086Issued February 03, 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 3007788086.

Observations4

Issue DateFebruary 03, 2016

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Chitogen, Inc.
Location: Plymouth, Minnesota, United States
FEI Number: 3007788086
Product Type: Devices
Issue Date: February 03, 2016
Country: United States

Inspection History, 2010 to 2024

NAI1

VAI4

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

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Chitogen, Inc. FDA Form 483, Plymouth, Minnesota, February 3, 2016