# UltraRad Corporation, Voorhees, NJ – FDA Inspections

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

> Inspection records and compliance data for UltraRad Corporation in Voorhees, New Jersey. 5 FDA inspections on record (1 OAI), 1 Form 483, last inspected August 18, 2023.

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## Details

- Name: UltraRad Corporation
- FEI Number: 3000149131
- Address Line 1: 1000 Haddonfield Berlin Rd Ste 209
- City: Voorhees
- State: New Jersey
- Zip Code: 08043
- Country Name: United States
- Address: 1000 Haddonfield Berlin Rd Ste 209, Voorhees, New Jersey 08043, United States
- Country: United States

## Related Documents

- FDA Inspection 1222755 - UltraRad Corporation - 2023-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2023
- FDA Inspection 1222755 - UltraRad Corporation - 2023-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2023
- FDA Inspection 1021969 - UltraRad Corporation - 2017-08-17 — classification: No Action Indicated (NAI), source: FDA, date: August 17, 2017
- [FDA Inspection 1021969 - UltraRad Corporation - 2017-08-17](https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/2dfdc003-af29-41c2-b1d3-803b897fb76e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 17, 2017
- [FDA Inspection 823495 - UltraRad Corporation - 2013-03-26](https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/68dabaff-3755-4e11-9811-65f5c56f2aae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 26, 2013
- FDA Inspection 659908 - UltraRad Corporation - 2010-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2010
- FDA Inspection 659908 - UltraRad Corporation - 2010-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2010
- [FDA Inspection 563822 - UltraRad Corporation - 2009-03-05](https://www.keypedia.com/records/fda_inspections/ultrarad-corporation/e02447b1-d0af-4506-8f07-29a61cde6dd6) — classification: Official Action Indicated (OAI), source: FDA, date: March 5, 2009
- FDA Inspection 563822 - UltraRad Corporation - 2009-03-05 — classification: Official Action Indicated (OAI), source: FDA, date: March 5, 2009

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