# FDA Inspection 993039 - Oticon A/S - November 11, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/oticon-as/db7085ec-73c2-42ba-b4bf-85004420611d
Source feed: FDA_Inspections

> FDA Inspection 993039 for Oticon A/S on November 11, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993039
- Company Name: Oticon A/S
- Inspection Date: 2016-11-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 993039 - 2016-11-11](https://www.globalkeysolutions.net/records/fda_inspections/oticon-as/9d10606c-a79d-48f3-988e-ea9d2ae5e11a)

Company: https://www.globalkeysolutions.net/companies/oticon-as/cc63530c-c60e-47c1-a9e9-4e6db8111e8e

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