# FDA Inspection 910418 - Willy Rusch GmbH a div of Teleflex Medical - December 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/willy-rusch-gmbh-a-div-of-teleflex-medical/5e55b20d-b4d8-446c-b7f1-7f96b4afd836
Source feed: FDA_Inspections

> FDA Inspection 910418 for Willy Rusch GmbH a div of Teleflex Medical on December 18, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 910418
- Company Name: Willy Rusch GmbH a div of Teleflex Medical
- Inspection Date: 2014-12-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 740152 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/willy-rusch-gmbh-a-div-of-teleflex-medical/974a3611-f01c-4ad7-8520-f525898364b2)
- [FDA Inspection 740152 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/willy-rusch-gmbh-a-div-of-teleflex-medical/8c78839d-5ca1-47eb-a9e4-3fe2dc0f64de)

Company: https://www.keypedia.com/companies/willy-rusch-gmbh-a-div-of-teleflex-medical/1ecd18f0-e80a-4c14-bf04-68886e6aa892

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