# FDA Inspection 933097 - August Reuchlen GmbH - July 02, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/august-reuchlen-gmbh/b1a2fcc1-f03e-4ab0-922b-9f4e69c6f8b1
Source feed: FDA_Inspections

> FDA Inspection 933097 for August Reuchlen GmbH on July 02, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 933097
- Company Name: August Reuchlen GmbH
- Inspection Date: 2015-07-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1270229 - 2025-05-02](https://www.globalkeysolutions.net/records/fda_inspections/august-reuchlen-gmbh/dc7ad8ff-799d-4c81-af4b-2134efd5972c)
- [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/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/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
