# FDA Inspection 791220 - Teleflex Medical, Inc. - July 19, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/teleflex-medical-inc/d965170f-5e76-49fb-ab2e-1b901b9756d6
Source feed: FDA_Inspections

> FDA Inspection 791220 for Teleflex Medical, Inc. on July 19, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 791220
- Company Name: Teleflex Medical, Inc.
- Inspection Date: 2012-07-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/teleflex-medical-inc/3b7f5b18-3093-426b-9b9c-be821e0caf75

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