# FDA Inspection 1100729 - Guy & O'Neill Inc. - August 22, 2019

Source: https://www.keypedia.com/records/fda_inspections/guy-oneill-inc/9ff6c234-58a7-4bb6-b652-91cee31d46c3
Source feed: FDA_Inspections

> FDA Inspection 1100729 for Guy & O'Neill Inc. on August 22, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100729
- Company Name: Guy & O'Neill Inc.
- Inspection Date: 2019-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100729 - 2019-08-22](https://www.keypedia.com/records/fda_inspections/guy-oneill-inc/9234b599-aa54-45f9-961b-77d36a4abed6)
- [FDA Inspection 1042033 - 2018-02-20](https://www.keypedia.com/records/fda_inspections/guy-oneill-inc/7ad9957d-ad94-400f-818d-717ef184fa88)

Company: https://www.keypedia.com/companies/guy-oneill-inc/786b6282-4f9d-4f5d-8752-6f612ed5fc24

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