# FDA Inspection 1029822 - Haussen, Diogo - September 26, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/haussen-diogo/20e0b00c-634c-4933-aeeb-ef58bf37d8d2
Source feed: FDA_Inspections

> FDA Inspection 1029822 for Haussen, Diogo on September 26, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029822
- Company Name: Haussen, Diogo
- Inspection Date: 2017-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/haussen-diogo/67d5e91d-e6ee-4383-a519-801b1578b979

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