# Teleflex Medical Tuttlingen GmbH – FDA Inspection, Nov 5, 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 of Teleflex Medical Tuttlingen GmbH, November 05, 2013. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 649050 - 2010-02-04

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