Airon Corporation

Form 483

Melbourne, Florida, United StatesFEI 3003697063Issued February 17, 2011

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 3003697063.

Observations7

Issue DateFebruary 17, 2011

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Airon Corporation
Location: Melbourne, Florida, United States
FEI Number: 3003697063
Product Type: Devices
Issue Date: February 17, 2011
Country: United States

Inspection History, 2011 to 2022

NAI1

VAI3

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

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Airon Corporation FDA Form 483, Melbourne, Florida, February 17, 2011