# FDA Inspection 931562 - Weinmann Gmbh - June 25, 2015

Source: https://www.keypedia.com/records/fda_inspections/weinmann-gmbh/5711be22-1f9b-4a44-97c6-2b010ea3d188
Source feed: FDA_Inspections

> FDA Inspection 931562 for Weinmann Gmbh on June 25, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931562
- Company Name: Weinmann Gmbh
- Inspection Date: 2015-06-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 698574 - 2010-10-21](https://www.keypedia.com/records/fda_inspections/weinmann-gmbh/b744f097-2293-41b1-9c57-462ca8cb949d)

Company: https://www.keypedia.com/companies/weinmann-gmbh/8e3aa4d5-66c2-45b9-9cf6-8838730d7bee

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7