# FDA Inspection 724020 - Vygon U.S.A. - April 14, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/vygon-usa/0fddae36-0c77-4b6b-9d44-3956b0661b5f
Source feed: FDA_Inspections

> FDA Inspection 724020 for Vygon U.S.A. on April 14, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 724020
- Company Name: Vygon U.S.A.
- Inspection Date: 2011-04-14
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/vygon-usa/971bb4ac-676f-4e1f-b676-a9bfdb41f7c3

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