# FDA Inspection 983531 - Novo Nordisk Inc. - July 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/novo-nordisk-inc/3f1b4ae6-1974-49b0-b186-49cb78cbf28b
Source feed: FDA_Inspections

> FDA Inspection 983531 for Novo Nordisk Inc. on July 22, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983531
- Company Name: Novo Nordisk Inc.
- Inspection Date: 2016-07-22
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/novo-nordisk-inc/920bb4ea-9450-45a6-bcd7-9f85c2f2bbad

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