PerioSeal, Inc.

Form 483

Little Rock, Arkansas, United StatesFEI 3005124408Issued August 09, 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 3005124408.

Observations5

Issue DateAugust 09, 2012

StatusNo Warning Letter

Related Inspections2

Establishment Details

Firm: PerioSeal, Inc.
Location: Little Rock, Arkansas, United States
FEI Number: 3005124408
Product Type: Devices
Issue Date: August 09, 2012
Country: United States

Inspection History, 2012 to 2013

VAI1

OAI1

VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

Act on This Form 483

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PerioSeal, Inc. FDA Form 483, Little Rock, Arkansas, August 9, 2012