FDA Inspection
Airon CorporationAiron Corporation – FDA Inspection, Jan 13, 2017
Record Details
This FDA Inspection record concerns Airon Corporation, with an inspection on January 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d621296f-d3e2-4de3-a663-488e18addbf9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1001776
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(e)Records of complaint investigation
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Airon Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 6, 2018 | Not classified | Florida District Office | |
| April 10, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 17, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Airon Corporation
- FDA Inspection 1178413 - 2022-08-04
- FDA Inspection 1105420 - 2018-11-06
- FDA Inspection 874350 - 2014-04-10
- FDA Inspection 710743 - 2011-02-17
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