# August Reuchlen GmbH – FDA Inspection, May 2, 2025

Source: https://www.keypedia.com/records/fda_inspections/august-reuchlen-gmbh/dc7ad8ff-799d-4c81-af4b-2134efd5972c
Source feed: FDA_Inspections

> FDA inspection 1270229 of August Reuchlen GmbH, May 02, 2025. 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: 1270229
- Company Name: August Reuchlen GmbH
- Inspection Date: 2025-05-02
- 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 Documents

- FDA Inspection 933097 - 2015-07-02

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/august-reuchlen-gmbh/9c0c3b5f-2ee2-4e98-ab6c-a52d3ea79a60

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