# FDA Inspection 683233 - Grayson O Company - August 05, 2010

Source: https://www.keypedia.com/records/fda_inspections/grayson-o-company/51d5ef0f-64c4-4f28-9aa9-77da2ebabdd0
Source feed: FDA_Inspections

> FDA Inspection 683233 for Grayson O Company on August 05, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 683233
- Company Name: Grayson O Company
- Inspection Date: 2010-08-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 767248 - 2012-02-08](https://www.keypedia.com/records/fda_inspections/grayson-o-company/95875386-555a-4b6c-9a58-1c794e32ee52)
- [FDA Inspection 683233 - 2010-08-05](https://www.keypedia.com/records/fda_inspections/grayson-o-company/6a3a1199-515b-4838-a779-dcc6b9fed5f9)
- [FDA Inspection 644533 - 2010-01-27](https://www.keypedia.com/records/fda_inspections/grayson-o-company/8e588fcb-7223-4209-97c9-5a9fd8cb1d98)
- [FDA Inspection 644533 - 2010-01-27](https://www.keypedia.com/records/fda_inspections/grayson-o-company/3ef25a16-2c64-4e3b-93aa-0c5e3c8ad431)

Company: https://www.keypedia.com/companies/grayson-o-company/0d6b93ee-3b2b-4724-bd9a-14de210f2926

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