# Agilent Technologies Denmark ApS – FDA Inspection, Mar 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 of Agilent Technologies Denmark ApS, March 14, 2013. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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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)
- Classification Code: OAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1080097 - 2018-05-18](https://www.keypedia.com/records/fda_inspections/agilent-technologies-denmark-aps/678bff9f-0275-4747-ab43-51482286f7d5)
- FDA Inspection 914699 - 2015-01-15

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