# Guy & O'Neill, Inc – FDA Inspection, Jan 26, 2011

Source: https://www.keypedia.com/records/fda_inspections/guy-oneill-inc/d96ca924-10e0-4fbc-9b59-d8697ad2a037
Source feed: FDA_Inspections

> FDA inspection 703350 of Guy & O'Neill, Inc, January 26, 2011. Classification: Voluntary Action Indicated (VAI). 12 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 703350
- Company Name: Guy & O'Neill, Inc
- Inspection Date: 2011-01-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 12

## Related Documents

- FDA Inspection 1022791 - 2017-07-25
- [FDA Inspection 964874 - 2016-02-12](https://www.keypedia.com/records/fda_inspections/guy-oneill-inc/4ad8a666-670e-474a-83d9-3b13c3bc0f92)
- FDA Inspection 871230 - 2014-03-21
- FDA Inspection 786218 - 2012-05-30

Company: https://www.keypedia.com/companies/guy-oneill-inc/b3197c60-0682-4714-a62e-b92a8e2a38ec

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