# Ormco/Sybronendo – FDA Inspection, Jun 29, 2011

Source: https://www.keypedia.com/records/fda_inspections/ormcosybronendo/8c83609a-4bf6-48cb-8766-8911fd4cce73
Source feed: FDA_Inspections

> FDA inspection 731636 of Ormco/Sybronendo, June 29, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 731636
- Company Name: Ormco/Sybronendo
- Inspection Date: 2011-06-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1031062 - 2017-07-21](https://www.keypedia.com/records/fda_inspections/ormcosybronendo/ba06a9d2-0e49-4892-abf3-533c1286dc95)
- FDA Inspection 763710 - 2012-01-24
- FDA Inspection 641489 - 2010-01-20

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

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