# FDA Inspection 1226587 - KAMEDI GMBH - December 13, 2023

Source: https://www.keypedia.com/records/fda_inspections/kamedi-gmbh/f4492e35-edc9-44ec-b260-f1086a3c7f0a
Source feed: FDA_Inspections

> FDA Inspection 1226587 for KAMEDI GMBH on December 13, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226587
- Company Name: KAMEDI GMBH
- Inspection Date: 2023-12-13
- 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/kamedi-gmbh/8e321e6b-fd11-4f9d-b879-a1a595d547b1

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