# Cablon Medical B.V. – FDA Inspection, Feb 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/cablon-medical-bv/a6018bc8-25a1-4cef-95e1-96b3648ce858
Source feed: FDA_Inspections

> FDA inspection 1197434 of Cablon Medical B.V., February 15, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197434
- Company Name: Cablon Medical B.V.
- Inspection Date: 2023-02-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 737692 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/cablon-medical-bv/10d3577c-85ed-482b-b751-038c4039e2c7)

## Related Officers

- [Investigator](https://www.keypedia.com/people/kevin-n-tran/dd74120c-4a8d-4fd0-9068-c862890d00d6)

Company: https://www.keypedia.com/companies/cablon-medical-bv/193fc8aa-9494-46bc-ba09-579d430b48d2

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