# Airon Corporation – FDA Inspection, Jan 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/airon-corporation/d621296f-d3e2-4de3-a663-488e18addbf9
Source feed: FDA_Inspections

> FDA inspection 1001776 of Airon Corporation, January 13, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1001776
- Company Name: Airon Corporation
- Inspection Date: 2017-01-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1178413 - 2022-08-04
- [FDA Inspection 1105420 - 2018-11-06](https://www.keypedia.com/records/fda_inspections/airon-corporation/48a38760-ca91-4a66-879b-394cdb5c3dbb)
- [FDA Inspection 874350 - 2014-04-10](https://www.keypedia.com/records/fda_inspections/airon-corporation/e262a8a1-2140-46f9-bfac-3123a29bc76c)
- FDA Inspection 710743 - 2011-02-17

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7