# FDA Inspection 1269787 - Relitech B.V. - May 01, 2025

Source: https://www.keypedia.com/records/fda_inspections/relitech-bv/d80a2b18-e439-4699-bdb8-52d6c9350242
Source feed: FDA_Inspections

> FDA Inspection 1269787 for Relitech B.V. on May 01, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1269787
- Company Name: Relitech B.V.
- Inspection Date: 2025-05-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1269787 - 2025-05-01](https://www.keypedia.com/records/fda_inspections/relitech-bv/e83bd8b7-50db-44b6-a122-704c1bcd3fbf)
- [FDA Inspection 1269787 - 2025-05-01](https://www.keypedia.com/records/fda_inspections/relitech-bv/1105b942-47a0-4add-9e16-8b42e4de3372)
- [FDA Inspection 1269787 - 2025-05-01](https://www.keypedia.com/records/fda_inspections/relitech-bv/bf6f47ed-d143-47c3-b8e4-77093bd57ed0)

Company: https://www.keypedia.com/companies/relitech-bv/652aef83-ac1a-48b6-a74a-14a9071d2498