Centrix, Inc.

Form 483

Shelton, Connecticut, United StatesFEI 1281412Issued January 31, 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 1281412.

Observations8

Issue DateJanuary 31, 2017

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Centrix, Inc.
Location: Shelton, Connecticut, United States
FEI Number: 1281412
Product Type: Drugs
Issue Date: January 31, 2017
Country: United States

Inspection History, 2010 to 2022

NAI2

VAI2

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

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Centrix, Inc. FDA Form 483, Shelton, Connecticut, January 31, 2017