# FDA Inspection 733405 - OraWell USA - August 05, 2011

Source: https://www.keypedia.com/records/fda_inspections/orawell-usa/ad879b1c-1d07-4f9b-afbc-bd5454491e63
Source feed: FDA_Inspections

> FDA Inspection 733405 for OraWell USA on August 05, 2011. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 733405
- Company Name: OraWell USA
- Inspection Date: 2011-08-05
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 762285 - 2011-12-15](https://www.keypedia.com/records/fda_inspections/orawell-usa/c3bc3927-057b-4865-8261-ea2154b21817)
- [FDA Inspection 733405 - 2011-08-05](https://www.keypedia.com/records/fda_inspections/orawell-usa/cbcac30b-46dc-4fa5-adc5-bafa64ed3419)

Company: https://www.keypedia.com/companies/orawell-usa/e2cbda70-7cb7-440c-86fe-f19848f0a2ae

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