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

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

> FDA inspection 1016703 of Vygon U.S.A., May 25, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 724020 - 2011-04-14](https://www.keypedia.com/records/fda_inspections/vygon-usa/3cf4d517-8c70-474b-9287-5a19f6fa343e)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)
- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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