# FDA Inspection 1226419 - AKTORmed GmbH - December 06, 2023

Source: https://www.keypedia.com/records/fda_inspections/aktormed-gmbh/c0deead4-d720-4036-bda7-c2e6bab11bb2
Source feed: FDA_Inspections

> FDA Inspection 1226419 for AKTORmed GmbH on December 06, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226419
- Company Name: AKTORmed GmbH
- Inspection Date: 2023-12-06
- 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/aktormed-gmbh/285761e9-87e4-43d0-a23b-c261ccf21396

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