# UltraRad Corporation – FDA Inspection, Aug 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/2dfdc003-af29-41c2-b1d3-803b897fb76e
Source feed: FDA_Inspections

> FDA inspection 1021969 of UltraRad Corporation, August 17, 2017. Classification: Voluntary Action Indicated (VAI). 3 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: 1021969
- Company Name: UltraRad Corporation
- Inspection Date: 2017-08-17
- 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: 3

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- [FDA Inspection 823495 - 2013-03-26](https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/68dabaff-3755-4e11-9811-65f5c56f2aae)
- FDA Inspection 659908 - 2010-05-10
- [FDA Inspection 563822 - 2009-03-05](https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/e02447b1-d0af-4506-8f07-29a61cde6dd6)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/loretta-nemchik/37791f6d-862a-4863-9295-1cca43f9fe3a)

Company: https://www.keypedia.com/companies/ultrarad-corporation/ac29a227-eea9-4dc8-8b5b-b8c1695020ba

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