# FDA Inspection 789814 - RH USA INC - July 16, 2012

Source: https://www.keypedia.com/records/fda_inspections/rh-usa-inc/05931713-93c2-4956-bdf6-8648fb6583e0
Source feed: FDA_Inspections

> FDA Inspection 789814 for RH USA INC on July 16, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 789814
- Company Name: RH USA INC
- Inspection Date: 2012-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1236262 - 2024-04-10](https://www.keypedia.com/records/fda_inspections/rh-usa-inc/2f0f2ecd-1a31-4b25-8270-b971274a98b9)
- [FDA Inspection 1236262 - 2024-04-10](https://www.keypedia.com/records/fda_inspections/rh-usa-inc/2ca30077-e07a-4a89-aa51-ec7b8af64c07)
- [FDA Inspection 1029403 - 2017-10-12](https://www.keypedia.com/records/fda_inspections/rh-usa-inc/50ef5fca-e65b-49e8-9ed2-a39bda05b88f)
- [FDA Inspection 1029403 - 2017-10-12](https://www.keypedia.com/records/fda_inspections/rh-usa-inc/55c05980-517c-4516-abce-0eb6c9050111)
- [FDA Inspection 1029403 - 2017-10-12](https://www.keypedia.com/records/fda_inspections/rh-usa-inc/3182a98f-cb26-49a9-927e-a4921874c5da)

Company: https://www.keypedia.com/companies/rh-usa-inc/6d6cb40d-34b3-44a4-b81a-6227695d15b3

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