# FDA Inspection 1029055 - Apriomed Ab - August 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/apriomed-ab/3275ccb3-fd70-42f1-9a87-32df667b154b
Source feed: FDA_Inspections

> FDA Inspection 1029055 for Apriomed Ab on August 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029055
- Company Name: Apriomed Ab
- Inspection Date: 2017-08-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/apriomed-ab/ea4dec7d-9ac8-4544-b46b-8e14e72ca8b3

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