# FDA Inspection 858921 - Teleflex Medical Tuttlingen GmbH - November 05, 2013

Source: https://www.keypedia.com/records/fda_inspections/teleflex-medical-tuttlingen-gmbh/740a7480-98cc-4289-95ca-ec837f50cdb4
Source feed: FDA_Inspections

> FDA Inspection 858921 for Teleflex Medical Tuttlingen GmbH on November 05, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 858921
- Company Name: Teleflex Medical Tuttlingen GmbH
- Inspection Date: 2013-11-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 649050 - 2010-02-04](https://www.keypedia.com/records/fda_inspections/teleflex-medical-tuttlingen-gmbh/a22d583a-ee23-47b7-9d98-7a7fd923965c)

Company: https://www.keypedia.com/companies/teleflex-medical-tuttlingen-gmbh/76535878-4c41-46d6-b1ac-3b8129d993a8

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