# EuropTec Polymer AG – FDA Inspection, Sep 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/europtec-polymer-ag/a56e2931-33f7-468e-9d15-b9053a3ee52e
Source feed: FDA_Inspections

> FDA inspection 1285196 of EuropTec Polymer AG, September 25, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1285196
- Company Name: EuropTec Polymer AG
- Inspection Date: 2025-09-25
- 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: 2

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

Company: https://www.keypedia.com/companies/europtec-polymer-ag/bdc14cce-8cd6-4d48-a16c-3ae7834fb6eb

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