# FDA Inspection 826561 - Agilent Technologies Denmark ApS - March 14, 2013

Source: https://www.keypedia.com/records/fda_inspections/agilent-technologies-denmark-aps/344996e8-d646-4f6e-a33e-0887e7f82b0d
Source feed: FDA_Inspections

> FDA Inspection 826561 for Agilent Technologies Denmark ApS on March 14, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 826561
- Company Name: Agilent Technologies Denmark ApS
- Inspection Date: 2013-03-14
- Classification: Official Action Indicated (OAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 914699 - 2015-01-15](https://www.keypedia.com/records/fda_inspections/agilent-technologies-denmark-aps/1dd2e386-cc37-478d-a6bc-5c7c2e309e71)

Company: https://www.keypedia.com/companies/agilent-technologies-denmark-aps/4c70874a-c0b0-46d4-ab49-6e72eda55961

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