# Relitech B.V. – FDA Inspection, May 1, 2025

Source: https://www.keypedia.com/records/fda_inspections/relitech-bv/1105b942-47a0-4add-9e16-8b42e4de3372
Source feed: FDA_Inspections

> FDA inspection 1269787 of Relitech B.V., May 01, 2025. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/juanj-wu/0d3e8970-b524-49f6-a307-079091b3c91d)

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8