# Ossur Americas, Foothill Ranch, CA – FDA Inspections

Source: https://www.keypedia.com/companies/ossur-americas/b99321db-aa98-4f20-aa2a-56979ac09053

> Inspection records and compliance data for Ossur Americas in Foothill Ranch, California. 6 FDA inspections on record, last inspected July 17, 2018.

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## Details

- Name: Ossur Americas
- FEI Number: 1000519909
- Address Line 1: 27051 Towne Centre Dr
- City: Foothill Ranch
- State: California
- Zip Code: 92610
- Country Name: United States
- Address: 27051 Towne Centre Dr, Foothill Ranch, California 92610, United States
- Country: United States

## Related Documents

- FDA Inspection 1063083 - Ossur Americas - 2018-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2018
- FDA Inspection 1063083 - Ossur Americas - 2018-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2018
- FDA Inspection 986687 - Ossur Americas - 2016-09-27 — classification: No Action Indicated (NAI), source: FDA, date: September 27, 2016
- [FDA Inspection 897335 - Ossur Americas - 2014-08-21](https://www.keypedia.com/records/fda_inspections/ossur-americas/999076b2-71f9-46a7-aab3-fbc69706acb7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 21, 2014
- FDA Inspection 897335 - Ossur Americas - 2014-08-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 21, 2014
- FDA Inspection 808387 - Ossur Americas - 2012-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2012
- FDA Inspection 808387 - Ossur Americas - 2012-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2012
- FDA Inspection 679074 - Ossur Americas - 2010-09-07 — classification: No Action Indicated (NAI), source: FDA, date: September 7, 2010
- FDA Inspection 552662 - Ossur Americas - 2008-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2008
- FDA Inspection 552662 - Ossur Americas - 2008-12-08 — classification: No Action Indicated (NAI), source: FDA, date: December 8, 2008

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