Airon Corporation

Form 483

Melbourne, Florida, United StatesFEI 3003697063Issued April 10, 2014

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.

Observations1

Issue DateApril 10, 2014

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Airon Corporation
Location: Melbourne, Florida, United States
FEI Number: 3003697063
Product Type: Devices
Issue Date: April 10, 2014
Country: United States

Inspection History, 2011 to 2022

NAI1

VAI3

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

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Airon Corporation FDA Form 483, Melbourne, Florida, April 10, 2014