# FDA Inspection 1264367 - VITROMED GmbH - February 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/vitromed-gmbh/70105856-5a57-4575-96e2-2beb5710d129
Source feed: FDA_Inspections

> FDA Inspection 1264367 for VITROMED GmbH on February 20, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1264367
- Company Name: VITROMED GmbH
- Inspection Date: 2025-02-20
- 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 1264367 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/vitromed-gmbh/e444ba84-0e7d-457e-a89f-ee9da774c0f4)
- [FDA Inspection 1264367 - 2025-02-20](https://www.keypedia.com/records/fda_inspections/vitromed-gmbh/3fb2a62c-d3c0-4376-8af6-8c6d037d6d91)

Company: https://www.keypedia.com/companies/vitromed-gmbh/e1cb485a-5089-42a5-b779-1608c8c2b5a1

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