# Puretone Ltd. – FDA Inspection, Nov 20, 2008

Source: https://www.keypedia.com/records/fda_inspections/puretone-ltd/8fffccd3-15ad-4c5d-9f44-f0f10ca68909
Source feed: FDA_Inspections

> FDA inspection 554189 of Puretone Ltd., November 20, 2008. Classification: Official Action Indicated (OAI). 10 citations under 21 CFR part 820.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

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