Acclarent, Inc.

Form 483

Irvine, California, United StatesFEI 3005172759Issued February 24, 2012

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 3005172759.

Observations3

Issue DateFebruary 24, 2012

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Acclarent, Inc.
Location: Irvine, California, United States
FEI Number: 3005172759
Product Type: Devices
Issue Date: February 24, 2012
Country: United States

Inspection History, 2012 to 2020

NAI1

VAI1

OAI2

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

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Acclarent, Inc. FDA Form 483, Irvine, California, February 24, 2012