# Vygon MFG, Inc. – FDA Inspection, Sep 23, 2016

Source: https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/b7b1eaac-6bb7-4928-83fb-e8cb72fa3a35
Source feed: FDA_Inspections

> FDA inspection 986397 of Vygon MFG, Inc., September 23, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 986397
- Company Name: Vygon MFG, Inc.
- Inspection Date: 2016-09-23
- 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 1054315 - 2018-05-21](https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/588d3aaa-53c1-4b58-82bb-1a9e57e4de14)
- FDA Inspection 848668 - 2013-09-05
- FDA Inspection 735332 - 2011-07-28
- FDA Inspection 702972 - 2010-12-17
- [FDA Inspection 577818 - 2009-02-18](https://www.keypedia.com/records/fda_inspections/vygon-mfg-inc/c58f3b8d-a5de-419c-a9fa-e4e511a1b743)

Company: https://www.keypedia.com/companies/vygon-mfg-inc/609245ef-6ebb-4020-8ef6-43be921cb444

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