# FDA Inspection 910408 - Teleflex Medical Gmbh - December 15, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-gmbh/dad32739-e06a-445f-af44-2ad5465b73b6
Source feed: FDA_Inspections

> FDA Inspection 910408 for Teleflex Medical Gmbh on December 15, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 910408
- Company Name: Teleflex Medical Gmbh
- Inspection Date: 2014-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/teleflex-medical-gmbh/10f5115b-f896-48c1-9f00-d0d1b7d6b573

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