# ILO Electronic GmbH – FDA Inspection, Sep 3, 2026

Source: https://www.keypedia.com/records/fda_inspections/ilo-electronic-gmbh/b73f85b2-e205-4366-8352-33095524088e
Source feed: FDA_Inspections

> FDA inspection 1334940 of ILO Electronic GmbH, September 03, 2026. Classification: Voluntary Action Indicated (VAI). 4 citations. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1334940
- Company Name: ILO Electronic GmbH
- Inspection Date: 2026-09-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 4

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sara-m-onyango/643c6ad3-9747-4bc2-9e8e-72f97b11e659)

Company: https://www.keypedia.com/companies/ilo-electronic-gmbh/b689e5ee-1b63-4bb0-a898-b11f77ac15a8

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