# FDA Inspection 1284368 - Rudolf Storz GmbH - September 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/rudolf-storz-gmbh/68e96a13-ee74-4e8a-a8e7-b39278cba5e0
Source feed: FDA_Inspections

> FDA Inspection 1284368 for Rudolf Storz GmbH on September 25, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1284368
- Company Name: Rudolf Storz GmbH
- Inspection Date: 2025-09-25
- 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 1284368 - 2025-09-25](https://www.keypedia.com/records/fda_inspections/rudolf-storz-gmbh/897ca4e4-9784-424b-8529-1d0b7dfc0bd0)
- [FDA Inspection 1284368 - 2025-09-25](https://www.keypedia.com/records/fda_inspections/rudolf-storz-gmbh/771d3fe4-2268-4b3a-9bb1-385c68c33553)
- [FDA Inspection 1284368 - 2025-09-25](https://www.keypedia.com/records/fda_inspections/rudolf-storz-gmbh/cab05808-c510-40e4-af01-3ca2fbd8a6b2)

Company: https://www.keypedia.com/companies/rudolf-storz-gmbh/887ac89d-f1c9-4463-8f21-6ca8186abb48

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