# FDA Inspection 554189 - Puretone Ltd. - November 20, 2008

Source: https://www.keypedia.com/records/fda_inspections/puretone-ltd/397e93a2-52ec-4ba2-88cd-1dc2e3f7a944
Source feed: FDA_Inspections

> FDA Inspection 554189 for Puretone Ltd. on November 20, 2008. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 554189
- Company Name: Puretone Ltd.
- Inspection Date: 2008-11-20
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 554189 - 2008-11-20](https://www.keypedia.com/records/fda_inspections/puretone-ltd/8fffccd3-15ad-4c5d-9f44-f0f10ca68909)

Company: https://www.keypedia.com/companies/puretone-ltd/6539fe49-ce3f-42e4-8c09-0cbbbd5166bd

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