# FDA Inspection 1270229 - August Reuchlen GmbH - May 02, 2025

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

> FDA Inspection 1270229 for August Reuchlen GmbH on May 02, 2025. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1270229 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/august-reuchlen-gmbh/ad47d5f9-d5e2-4cb2-8d1e-b104f7ef034c)
- [FDA Inspection 933097 - 2015-07-02](https://www.globalkeysolutions.net/records/fda_inspections/august-reuchlen-gmbh/b1a2fcc1-f03e-4ab0-922b-9f4e69c6f8b1)
- [FDA Inspection 933097 - 2015-07-02](https://www.globalkeysolutions.net/records/fda_inspections/august-reuchlen-gmbh/05bab278-76e7-4690-81e8-21ad4c211564)

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

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