# Vygon U.S.A. – FDA Inspection, Apr 14, 2011

Source: https://www.keypedia.com/records/fda_inspections/vygon-usa/3cf4d517-8c70-474b-9287-5a19f6fa343e
Source feed: FDA_Inspections

> FDA inspection 724020 of Vygon U.S.A., April 14, 2011. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1016703 - 2017-05-25](https://www.keypedia.com/records/fda_inspections/vygon-usa/da75f1d5-947a-4285-b696-7db67d99d083)

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

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