# FDA Inspection 1025854 - Teleflex Medical, Inc. - September 20, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/dd0fc511-d6d3-43d5-9d87-ea8cd8dc0395
Source feed: FDA_Inspections

> FDA Inspection 1025854 for Teleflex Medical, Inc. on September 20, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025854
- Company Name: Teleflex Medical, Inc.
- Inspection Date: 2017-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025854 - 2017-09-20](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/9e2bcd1f-862a-4c68-a557-01ddbc8814f6)
- [FDA Inspection 806348 - 2012-10-24](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/9b96076e-b66c-4edc-bd54-b03928e3beae)
- [FDA Inspection 609930 - 2009-08-27](https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/1c057bdf-c88f-495b-8f86-3bbc43c38e9a)

Company: https://www.globalkeysolutions.net/companies/teleflex-medical-inc/ccdcbad7-c558-42ab-b8da-d80880728b5f

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