# Phonak Ag – FDA Inspection, Sep 8, 2016

Source: https://www.keypedia.com/records/fda_inspections/phonak-ag/738ce1ce-dcd4-4199-8ffc-f847880685c6
Source feed: FDA_Inspections

> FDA inspection 988558 of Phonak Ag, September 08, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 988558
- Company Name: Phonak Ag
- Inspection Date: 2016-09-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

Company: https://www.keypedia.com/companies/phonak-ag/2a9d9808-513c-4ead-9ca1-23ae62fe21b5

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