# FDA Inspection 829270 - Novo Nordisk A/S - 25a-B - March 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/novo-nordisk-as-25a-b/03cc787e-f2a0-4966-9bcd-3d7d207ff282
Source feed: FDA_Inspections

> FDA inspection 829270 of Novo Nordisk A/S - 25a-B, March 19, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 829270
- Company Name: Novo Nordisk A/S - 25a-B
- Inspection Date: 2013-03-19
- 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: 2

## Related Documents

- [FDA Inspection 1223821 - 2023-11-07](https://www.keypedia.com/records/fda_inspections/novo-nordisk-as-25a-b/1311c640-239f-42db-a99a-a4b693406f50)
- FDA Inspection 1207487 - 2022-11-04
- FDA Inspection 1118196 - 2018-06-14
- FDA Inspection 957571 - 2016-01-22
- FDA Inspection 933969 - 2015-06-18

Company: https://www.keypedia.com/companies/novo-nordisk-as-25a-b/017e6784-9871-4c62-9884-314e60ba61b7

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