# FDA Inspection 784308 - THEROZONE USA, INC. - May 31, 2012

Source: https://www.keypedia.com/records/fda_inspections/therozone-usa-inc/61150702-58be-4df3-a17a-1acf29833a93
Source feed: FDA_Inspections

> FDA Inspection 784308 for THEROZONE USA, INC. on May 31, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 784308
- Company Name: THEROZONE USA, INC.
- Inspection Date: 2012-05-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 712827 - 2011-03-16](https://www.keypedia.com/records/fda_inspections/therozone-usa-inc/d1afcea9-b601-40d8-b330-12286fab24d5)
- [FDA Inspection 712827 - 2011-03-16](https://www.keypedia.com/records/fda_inspections/therozone-usa-inc/369a8716-9dcd-462d-b84d-1de9fef33a98)

Company: https://www.keypedia.com/companies/therozone-usa-inc/ac63654e-a5ae-4d2f-9220-949cd22a2049

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