# Ormco/Sybronendo, Glendora, CA – FDA Inspections

Source: https://www.keypedia.com/companies/ormcosybronendo/0426de4f-aa4d-4880-8752-521e95ec8eeb

> Inspection records and compliance data for Ormco/Sybronendo in Glendora, California. 4 FDA inspections on record, 1 Form 483, last inspected July 21, 2017.

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## Details

- Name: Ormco/Sybronendo
- FEI Number: 2016150
- Address Line 1: 1332 S Lone Hill Ave
- City: Glendora
- State: California
- Zip Code: 91740
- Country Name: United States
- Address: 1332 S Lone Hill Ave, Glendora, California 91740, United States
- Country: United States

## Related Documents

- [FDA Inspection 1031062 - Ormco/Sybronendo - 2017-07-21](https://www.keypedia.com/records/fda_inspections/ormcosybronendo/ba06a9d2-0e49-4892-abf3-533c1286dc95) — source: FDA, date: July 21, 2017
- FDA Inspection 763710 - Ormco/Sybronendo - 2012-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2012
- FDA Inspection 763710 - Ormco/Sybronendo - 2012-01-24 — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2012
- FDA Inspection 731636 - Ormco/Sybronendo - 2011-06-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- [FDA Inspection 731636 - Ormco/Sybronendo - 2011-06-29](https://www.keypedia.com/records/fda_inspections/ormcosybronendo/8c83609a-4bf6-48cb-8766-8911fd4cce73) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2011
- FDA Inspection 641489 - Ormco/Sybronendo - 2010-01-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 20, 2010

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