# Ortho Development Corporation, Draper, UT – FDA Inspections

Source: https://www.keypedia.com/companies/ortho-development-corporation/806e6b13-b860-41d7-a853-e90a844fe86d

> Inspection records and compliance data for Ortho Development Corporation in Draper, Utah. 5 FDA inspections on record, last inspected July 19, 2021.

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## Details

- Name: Ortho Development Corporation
- FEI Number: 1000143502
- Address Line 1: 12187 S Business Park Dr
- City: Draper
- State: Utah
- Zip Code: 84020
- Country Name: United States
- Address: 12187 S Business Park Dr, Draper, Utah 84020, United States
- Country: United States

## Related Documents

- FDA Inspection 1149215 - Ortho Development Corporation - 2021-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2021
- FDA Inspection 990045 - Ortho Development Corporation - 2016-10-04 — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2016
- FDA Inspection 990045 - Ortho Development Corporation - 2016-10-04 — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2016
- FDA Inspection 927114 - Ortho Development Corporation - 2015-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2015
- FDA Inspection 927114 - Ortho Development Corporation - 2015-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2015
- FDA Inspection 858180 - Ortho Development Corporation - 2013-12-10 — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2013
- FDA Inspection 858180 - Ortho Development Corporation - 2013-12-10 — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2013
- FDA Inspection 728478 - Ortho Development Corporation - 2011-06-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2011
- FDA Inspection 728478 - Ortho Development Corporation - 2011-06-03 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 3, 2011
- FDA Inspection 728478 - Ortho Development Corporation - 2011-06-03 — classification: No Action Indicated (NAI), source: FDA, date: June 3, 2011

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