# Airon Corporation, Melbourne, FL – FDA Inspections

Source: https://www.keypedia.com/companies/airon-corporation/9e023f1b-3db4-4a14-bde6-9ae257ab0d07

> Inspection records and compliance data for Airon Corporation in Melbourne, Florida. 5 FDA inspections on record, 2 Form 483s, last inspected August 04, 2022.

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## Details

- Name: Airon Corporation
- FEI Number: 3003697063
- Address Line 1: 751 North Dr Ste 6
- City: Melbourne
- State: Florida
- Zip Code: 32934
- Country Name: United States
- Address: 751 North Dr Ste 6, Melbourne, Florida 32934, United States
- Country: United States

## Related Documents

- FDA Inspection 1178413 - Airon Corporation - 2022-08-04 — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2022
- FDA Inspection 1178413 - Airon Corporation - 2022-08-04 — classification: No Action Indicated (NAI), source: FDA, date: August 4, 2022
- [FDA Inspection 1105420 - Airon Corporation - 2018-11-06](https://www.keypedia.com/records/fda_inspections/airon-corporation/48a38760-ca91-4a66-879b-394cdb5c3dbb) — source: FDA, date: November 6, 2018
- FDA Inspection 1001776 - Airon Corporation - 2017-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2017
- [FDA Inspection 1001776 - Airon Corporation - 2017-01-13](https://www.keypedia.com/records/fda_inspections/airon-corporation/d621296f-d3e2-4de3-a663-488e18addbf9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2017
- [FDA Inspection 874350 - Airon Corporation - 2014-04-10](https://www.keypedia.com/records/fda_inspections/airon-corporation/e262a8a1-2140-46f9-bfac-3123a29bc76c) — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2014
- FDA Inspection 874350 - Airon Corporation - 2014-04-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2014
- FDA Inspection 710743 - Airon Corporation - 2011-02-17 — classification: No Action Indicated (NAI), source: FDA, date: February 17, 2011
- FDA Inspection 710743 - Airon Corporation - 2011-02-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 17, 2011

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