# FDA Inspection 1016703 - Vygon U.S.A. - May 25, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/vygon-usa/da75f1d5-947a-4285-b696-7db67d99d083
Source feed: FDA_Inspections

> FDA Inspection 1016703 for Vygon U.S.A. on May 25, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1016703
- Company Name: Vygon U.S.A.
- Inspection Date: 2017-05-25
- 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