# FDA Inspection 1250923 - Strub Medical GmbH & Co. KG - September 26, 2024

Source: https://www.keypedia.com/records/fda_inspections/strub-medical-gmbh-co-kg/826b5e57-68fa-442c-9b0a-2de6917ceeb5
Source feed: FDA_Inspections

> FDA Inspection 1250923 for Strub Medical GmbH & Co. KG on September 26, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250923
- Company Name: Strub Medical GmbH & Co. KG
- Inspection Date: 2024-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1250923 - 2024-09-26](https://www.keypedia.com/records/fda_inspections/strub-medical-gmbh-co-kg/a1bf50da-a7f8-4231-9dcc-b8f7657a34d9)
- [FDA Inspection 1250923 - 2024-09-26](https://www.keypedia.com/records/fda_inspections/strub-medical-gmbh-co-kg/a021c014-105e-4238-9f28-66fdff3f144c)

Company: https://www.keypedia.com/companies/strub-medical-gmbh-co-kg/ce65f9e2-780a-4a8a-8c92-fc270d26ced3

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