# FDA Inspection 1005908 - IVF Hartmann AG - January 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/ivf-hartmann-ag/40fc1cd1-f32d-4dab-a382-18c4c207880d
Source feed: FDA_Inspections

> FDA Inspection 1005908 for IVF Hartmann AG on January 31, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005908
- Company Name: IVF Hartmann AG
- Inspection Date: 2017-01-31
- 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/ivf-hartmann-ag/85b1f1e1-bc2f-4d2f-8d63-9952ed8ce804

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